Canonical Allele Identifier: PA2830270406
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 1217279
ClinVar RCV Id: RCV001582388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620576.1:p.Tyr143del
CA3666717
NM_139007.3:c.427_429del