Canonical Allele Identifier: PA105083
Gene: HFE HGNC NCBI
ClinVar RCV:
RCV000000030
ClinVar Variation:
13
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000401.1:p.Gly93Arg
CA280943
NM_000410.4:c.277G>C
CA363206071
NM_000410.4:c.277G>A