Allele Registry

Canonical Allele Identifier: PA121454

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000012196

RCV002307362

ClinVar Variation:

11443

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032900.1:p.Leu122Val	CA121451 NM_001037811.2:c.364C>G