Canonical Allele Identifier: PA2830270762
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2272308
ClinVar RCV Id: RCV002799735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620578.1:p.Tyr208Cys
CA363207806
NM_139009.3:c.623A>G