Allele Registry

Canonical Allele Identifier: PA121466

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000012199

ClinVar Variation:

11446

HGVS (amino-acid)	Matching Registered Transcripts
NP_004484.1:p.Glu249Gln	CA121462 NM_004493.3:c.745G>C