Canonical Allele Identifier: PA2830269995
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2692107
ClinVar RCV Id: RCV003494304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620573.1:p.Pro116Ala
CA363207547
NM_139004.3:c.346C>G