Canonical Allele Identifier: PA2830270556
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 356195
ClinVar RCV Id: RCV000348043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620577.1:p.Thr134Ile
CA3666724
NM_139008.3:c.401C>T