Canonical Allele Identifier: PA645407573
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 356195
ClinVar RCV Id: RCV000348043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000401.1:p.Thr236Ile
CA3666724
NM_000410.4:c.707C>T