Canonical Allele Identifier: PA2830270760
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 1217279
ClinVar RCV Id: RCV001582388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620578.1:p.Tyr208del
CA3666717
NM_139009.3:c.622_624del