Canonical Allele Identifier: PA2830270250
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 356195
ClinVar RCV Id: RCV000348043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620575.1:p.Thr222Ile
CA3666724
NM_139006.3:c.665C>T