D38G (p.Asp38Gly) variant of PDE6B (P35913)
D38G (p.Asp38Gly) in PDE6B (P35913) is a missense change. The record also includes structural context.
D38G (p.Asp38Gly) variant details
- p.Asp38Gly
- gnomAD rs1734055830
- Missense
- Structural context available
D38G (p.Asp38Gly) in PDE6B (P35913) is a missense change. The record also includes structural context.