Canonical Allele Identifier: PA2830270766
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 356195
ClinVar RCV Id: RCV000348043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620578.1:p.Thr213Ile
CA3666724
NM_139009.3:c.638C>T