Canonical Allele Identifier: PA2830269860
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2539469
ClinVar RCV Id: RCV003292086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620572.1:p.Ile190Thr
CA363208818
NM_139003.3:c.569T>C