Canonical Allele Identifier: PA916018925
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 9

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287678.1:p.Cys282Tyr
CA113795
NM_001300749.2:c.845G>A