Y50C (p.Tyr50Cys) variant of ATP13A2 (Q9NQ11)
Y50C (p.Tyr50Cys) in ATP13A2 (Q9NQ11) is a missense change. The record also includes structural context.
Y50C (p.Tyr50Cys) variant details
- p.Tyr50Cys
- TOPMed rs916488046
- Missense
- Structural context available