Canonical Allele Identifier: PA2826848256
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 11

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287678.1:p.Ser65Cys
CA339778
NM_001300749.2:c.193A>T