Allele Registry

Canonical Allele Identifier: PA105620

Gene: HSD17B3 HGNC NCBI

ClinVar RCV:

RCV000005151

RCV000584321

RCV000623499

RCV001804713

ClinVar Variation:

4875

HGVS (amino-acid)	Matching Registered Transcripts
NP_000188.1:p.Ala203Val	CA117113 NM_000197.2:c.608C>T