Canonical Allele Identifier: PA2826848329
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2919212
ClinVar RCV Id: RCV003751581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287678.1:p.Ala227Pro
CA363207751
NM_001300749.2:c.679G>C