Canonical Allele Identifier: PA2828939067
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2272308
ClinVar RCV Id: RCV002799735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371093.1:p.Tyr231Cys
CA363207806
NM_001384164.1:c.692A>G