Canonical Allele Identifier: PA2828524730
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937767
ClinVar RCV Id: RCV003794397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361427.1:p.Ala196Glu
CA360866385
NM_001374498.1:c.587C>A