Canonical Allele Identifier: PA2830270665
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 11

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620578.1:p.Ser42Cys
CA339778
NM_139009.3:c.124A>T