Allele Registry

Canonical Allele Identifier: PA170596

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000133540

ClinVar Variation:

144033

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032900.1:p.Asp86Gly	CA170593 NM_001037811.2:c.257A>G