"Mendelics"[submitter] AND "HPD"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1576	NM_002150.3(HPD):c.1005C>G (p.Ile335Met)	HPD (I335M +1 more)	Single nucleotide variant (missense variant)	HPD-related condition +4 more	GConflicting classifications of pathogenicity
Select item 802899	NM_002150.3(HPD):c.97A>G (p.Thr33Ala)	HPD (T33A)	Single nucleotide variant (5 prime UTR variant +1 more)	Hawkinsinuria +2 more	GBenign