D19G (p.Asp19Gly) variant of PIM1 (P11309)
D19G (p.Asp19Gly) in PIM1 (P11309) is a missense change. The record also includes structural context.
D19G (p.Asp19Gly) variant details
- p.Asp19Gly
- TOPMed rs1762257677
- Missense
- Structural context available
D19G (p.Asp19Gly) in PIM1 (P11309) is a missense change. The record also includes structural context.