Canonical Allele Identifier: PA916071746
Gene: HFE HGNC NCBI
ClinVar RCV:
RCV000000035
ClinVar Variation:
18
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620580.1:p.Arg58Met
CA280947
NM_139011.3:c.173G>T