Canonical Allele Identifier: PA2826848319
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2692107
ClinVar RCV Id: RCV003494304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287678.1:p.Pro208Ala
CA363207547
NM_001300749.2:c.622C>G