Canonical Allele Identifier: PA2830269818
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 959749
ClinVar RCV Id: RCV001233153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620572.1:p.Asp136Asn
CA136292908
NM_139003.3:c.406G>A