F39C (p.Phe39Cys) variant of NFE2L2 (Q16236)
F39C (p.Phe39Cys) in NFE2L2 (Q16236) is a missense change. The record also includes structural context.
F39C (p.Phe39Cys) variant details
- p.Phe39Cys
- TOPMed rs1689663068
- Missense
- Structural context available