Canonical Allele Identifier: PA095367
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 11444
ClinVar RCV Id: RCV000012197

Amino-acid Alleles

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