Canonical Allele Identifier: PA916071708
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_620577.1:p.Gln39His
CA280945
NM_139008.3:c.117A>C
CA363206484
NM_139008.3:c.117A>T