Allele Registry

Canonical Allele Identifier: PA105662

Gene: HSD17B3 HGNC NCBI

ClinVar RCV:

RCV000005156

RCV001818138

ClinVar Variation:

4880

HGVS (amino-acid)	Matching Registered Transcripts
NP_000188.1:p.Asn130Ser	CA117116 NM_000197.2:c.389A>G