Canonical Allele Identifier: PA2830270476
Gene: HFE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620576.1:p.Arg242Met
CA280947
NM_139007.3:c.725G>T