Canonical Allele Identifier: PA645497749
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 435470
ClinVar RCV Id: RCV000504036 RCV000766098 RCV001857111 RCV004023377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004484.1:p.Val87Ile
CA10421022
NM_004493.3:c.259G>A