G56S (p.Gly56Ser) variant of SCN9A (Nav1.7)
G56S (p.Gly56Ser) in SCN9A (Nav1.7) is a missense change. The record also includes structural context.
G56S (p.Gly56Ser) variant details
- p.Gly56Ser
- TOPMed rs1698961116
- Missense
- Structural context available
G56S (p.Gly56Ser) in SCN9A (Nav1.7) is a missense change. The record also includes structural context.