D41N (p.Asp41Asn) variant of HFE (Q30201)
D41N (p.Asp41Asn) in HFE (Q30201) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary hemochromatosis. The record also includes structural context.
D41N (p.Asp41Asn) variant details
- p.Asp41Asn
- Ensembl rs1762647785
- Uncertain significance
- Hereditary hemochromatosis
- Missense
- ClinVar: Uncertain significance (Hereditary hemochromatosis)
- UniProt: Uncertain significance
- Structural context available