Canonical Allele Identifier: PA2830270455
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 461195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620576.1:p.Val207Ala
CA3666752
NM_139007.3:c.620T>C