Canonical Allele Identifier: PA2830270296
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 461195
ClinVar RCV Id: RCV000729729 RCV001085995 RCV001152293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620575.1:p.Val281Ala
CA3666752
NM_139006.3:c.842T>C