Canonical Allele Identifier: PA105009
Gene: HFE HGNC NCBI
ClinVar RCV:
RCV000000035
ClinVar Variation:
18
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000401.1:p.Arg330Met
CA280947
NM_000410.4:c.989G>T