Canonical Allele Identifier: PA2825163851
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 2692107
ClinVar RCV Id: RCV003494304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000401.1:p.Pro208Ala
CA363207547
NM_000410.4:c.622C>G