Canonical Allele Identifier: PA2580511977
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2272308
ClinVar RCV Id: RCV002799735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620579.1:p.Tyr51Cys
CA363207806
NM_139010.3:c.152A>G