Canonical Allele Identifier: PA2830270182
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 17
ClinVar RCV Id: RCV000000034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620575.1:p.Gln127His
CA280945
NM_139006.3:c.381A>C
CA363206484
NM_139006.3:c.381A>T