NM_207309.3(UAP1L1):c.1262G>A (p.Arg421His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004365881.1
Allele description [Variation Report for NM_207309.3(UAP1L1):c.1262G>A (p.Arg421His)]
NM_207309.3(UAP1L1):c.1262G>A (p.Arg421His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
gap junction alpha-3 protein isoform X1 [Homo sapiens]
gap junction alpha-3 protein isoform X1 [Homo sapiens]gi|767977600|ref|XP_011533350.1|Protein
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Last Updated: Oct 26, 2024