G47W (p.Gly47Trp) variant of KMT2D (O14686)
G47W (p.Gly47Trp) in KMT2D (O14686) is a missense change. The record also includes structural context.
G47W (p.Gly47Trp) variant details
- p.Gly47Trp
- TOPMed rs1938317391
- Missense
- Structural context available
G47W (p.Gly47Trp) in KMT2D (O14686) is a missense change. The record also includes structural context.