V33G (p.Val33Gly) variant of SCN4A (Nav1.4)
V33G (p.Val33Gly) in SCN4A (Nav1.4) is a missense change. The record also includes structural context.
V33G (p.Val33Gly) variant details
- p.Val33Gly
- TOPMed rs921149749
- gnomAD rs921149749
- Missense
- Structural context available