Allele Registry

Canonical Allele Identifier: PA121458

Gene: HSD17B10 HGNC NCBI

ClinVar RCV:

RCV000012197

ClinVar Variation:

11444

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032900.1:p.Asn238Ser	CA121455 NM_001037811.2:c.713A>G