Canonical Allele Identifier: PA1139747840
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 970730
ClinVar RCV Id: RCV001246359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620575.1:p.Gly36Asp
CA363204053
NM_139006.3:c.107G>A