Canonical Allele Identifier: PA2830269812
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 356195
ClinVar RCV Id: RCV000348043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620572.1:p.Thr130Ile
CA3666724
NM_139003.3:c.389C>T