Canonical Allele Identifier: PA2830269973
Gene: HFE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620573.1:p.Gly93Arg
CA280943
NM_139004.3:c.277G>C
CA363206071
NM_139004.3:c.277G>A