Canonical Allele Identifier: PA916071738
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 356195
ClinVar RCV Id: RCV000348043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620579.1:p.Thr56Ile
CA3666724
NM_139010.3:c.167C>T