Allele Registry

Canonical Allele Identifier: PA105630

Gene: HSD17B3 HGNC NCBI

ClinVar RCV:

RCV000005155

ClinVar Variation:

4879

HGVS (amino-acid)	Matching Registered Transcripts
NP_000188.1:p.Ala56Thr	CA117115 NM_000197.2:c.166G>A