Canonical Allele Identifier: PA2828939066
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 1217279
ClinVar RCV Id: RCV001582388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371093.1:p.Tyr231del
CA3666717
NM_001384164.1:c.691_693del