Allele Registry

Canonical Allele Identifier: PA105713

Gene: HSD17B3 HGNC NCBI

ClinVar RCV:

RCV000255975

RCV000583165

RCV001267038

ClinVar Variation:

265484

HGVS (amino-acid)	Matching Registered Transcripts
NP_000188.1:p.Pro282Leu	CA5140241 NM_000197.2:c.845C>T