Allele Registry

Canonical Allele Identifier: PA105677

Gene: HSD17B3 HGNC NCBI

ClinVar RCV:

RCV000005157

ClinVar Variation:

4881

HGVS (amino-acid)	Matching Registered Transcripts
NP_000188.1:p.Cys268Tyr	CA117117 NM_000197.2:c.803G>A