heterogeneous nuclear ribonucleoprotein H isoform a [Homo sapiens]

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HNRNPH1-related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome. [Clin Genet. 2020]
HNRNPH1-related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome.
Reichert SC, Li R, A Turner S, van Jaarsveld RH, Massink MPG, van den Boogaard MH, Del Toro M, Rodríguez-Palmero A, Fourcade S, Schlüter A, et al. Clin Genet. 2020 Jul; 98(1):91-98. Epub 2020 May 15.
Coding and noncoding drivers of mantle cell lymphoma identified through exome and genome sequencing. [Blood. 2020]
Coding and noncoding drivers of mantle cell lymphoma identified through exome and genome sequencing.
Pararajalingam P, Coyle KM, Arthur SE, Thomas N, Alcaide M, Meissner B, Boyle M, Qureshi Q, Grande BM, Rushton C, et al. Blood. 2020 Jul 30; 136(5):572-584.
Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation. [Clin Genet. 2018]
Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation.
Pilch J, Koppolu AA, Walczak A, Murcia Pienkowski VA, Biernacka A, Skiba P, Machnik-Broncel J, Gasperowicz P, Kosińska J, Rydzanicz M, et al. Clin Genet. 2018 Oct; 94(3-4):381-385. Epub 2018 Aug 2.

RefSeq mRNA
See reference mRNA sequence for the HNRNPH1 gene (NM_001364238.2).
RefSeq protein isoforms
See 52 reference sequence protein isoforms for the HNRNPH1 gene.

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Protein