Allele Registry

Canonical Allele Identifier: PA121450

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000012195

RCV001224055

ClinVar Variation:

11442

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032900.1:p.Arg130Cys	CA121447 NM_001037811.2:c.388C>T