Canonical Allele Identifier: PA658660269
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 452680
ClinVar RCV Id: RCV000519340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000401.1:p.Arg71Gln
CA3666613
NM_000410.4:c.212G>A