Allele Registry

Canonical Allele Identifier: PA095367

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000012197

ClinVar Variation:

11444

HGVS (amino-acid)	Matching Registered Transcripts
NP_004484.1:p.Asn247Ser	CA121455 NM_004493.3:c.740A>G