Allele Registry

Canonical Allele Identifier: PA222736

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000081106

RCV000488826

ClinVar Variation:

95101

HGVS (amino-acid)	Matching Registered Transcripts
NP_004484.1:p.Val65Ala	CA222732 NM_004493.3:c.194T>C