Canonical Allele Identifier: PA916071708
Gene: HFE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

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