Canonical Allele Identifier: PA2741870956
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937767
ClinVar RCV Id: RCV003794397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361428.1:p.Ala87Glu
CA360866385
NM_001374499.1:c.260C>A