Allele Registry

Canonical Allele Identifier: PA121465

Gene: HSD17B10 HGNC NCBI

ClinVar Allele:

26485

ClinVar RCV:

RCV000012199

ClinVar Variation:

11446

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032900.1:p.Glu240Gln	CA121462 NM_001037811.2:c.718G>C