Canonical Allele Identifier: PA2826239695
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 504931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Cys40Tyr
CA3381664
NM_001199291.3:c.119G>A