Canonical Allele Identifier: PA2830269859
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 461195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620572.1:p.Val189Ala
CA3666752
NM_139003.3:c.566T>C