Allele Registry

Canonical Allele Identifier: PA105732

Gene: HSD17B3 HGNC NCBI

ClinVar RCV:

RCV004555548

ClinVar Variation:

242504

HGVS (amino-acid)	Matching Registered Transcripts
NP_000188.1:p.Ser65Leu	CA351299 NM_000197.2:c.194C>T