F47C (p.Phe47Cys) variant of MEN1 (Menin)
F47C (p.Phe47Cys) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
F47C (p.Phe47Cys) variant details
- p.Phe47Cys
- Ensembl rs2136192635
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available