Canonical Allele Identifier: PA916071706
Gene: HFE HGNC NCBI
ClinVar RCV:
RCV000000030
ClinVar Variation:
13
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620575.1:p.Gly93Arg
CA280943
NM_139006.3:c.277G>C
CA363206071
NM_139006.3:c.277G>A