Canonical Allele Identifier: PA2830270105
Gene: HFE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620573.1:p.Arg238Met
CA280947
NM_139004.3:c.713G>T