Canonical Allele Identifier: PA2830270627
Gene: HFE HGNC NCBI
ClinVar RCV:
RCV000000035
ClinVar Variation:
18
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620577.1:p.Arg228Met
CA280947
NM_139008.3:c.683G>T