Canonical Allele Identifier: PA2830269852
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 9
ClinVar RCV Id: RCV000000019 RCV000178096 RCV000210820 RCV000308358 RCV000414811 RCV001248830 RCV001270034 RCV001731264 RCV002280089 RCV002512585 RCV003224084 RCV003493406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620572.1:p.Cys176Tyr
CA113795
NM_139003.3:c.527G>A