Canonical Allele Identifier: PA2826848282
Gene: HFE HGNC NCBI
ClinVar RCV:
RCV000000034
ClinVar Variation:
17
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287678.1:p.Gln127His
CA280945
NM_001300749.2:c.381A>C
CA363206484
NM_001300749.2:c.381A>T