Canonical Allele Identifier: PA2826848335
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 356195
ClinVar RCV Id: RCV000348043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287678.1:p.Thr236Ile
CA3666724
NM_001300749.2:c.707C>T