Canonical Allele Identifier: PA2830269720
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 216425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620572.1:p.Arg6Ser
CA338954
NM_139003.3:c.18G>C
CA363202632
NM_139003.3:c.18G>T