Canonical Allele Identifier: PA916071671
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 10

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620575.1:p.His63Asp
CA113797
NM_139006.3:c.187C>G