Canonical Allele Identifier: PA2828524731
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361427.1:p.Ala196Val
CA3381883
NM_001374498.1:c.587C>T