Canonical Allele Identifier: PA2830270685
Gene: HFE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620578.1:p.Gly70Arg
CA280943
NM_139009.3:c.208G>C
CA363206071
NM_139009.3:c.208G>A