Canonical Allele Identifier: PA2830269769
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 11

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620572.1:p.Ser65Cys
CA339778
NM_139003.3:c.193A>T