S2C (p.Ser2Cys) variant of CUL3 (Cullin-3)
S2C (p.Ser2Cys) in CUL3 (Cullin-3) is a missense change. Clinical records describe it as []. The record also includes structural context.
S2C (p.Ser2Cys) variant details
- p.Ser2Cys
- rs908831506
- []
- Missense
- Structural context available