Canonical Allele Identifier: PA2826848251
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 16

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287678.1:p.Val59Met
CA113804
NM_001300749.2:c.175G>A