Allele Registry

Canonical Allele Identifier: PA645497921

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000240845

ClinVar Variation:

254239

HGVS (amino-acid)	Matching Registered Transcripts
NP_004484.1:p.Pro198Thr	CA10586376 NM_004493.3:c.592C>A