A11G (p.Ala11Gly) variant of MYD88 (Q99836)
A11G (p.Ala11Gly) in MYD88 (Q99836) is a missense change. The record also includes structural context.
A11G (p.Ala11Gly) variant details
- p.Ala11Gly
- ExAC rs777249439
- gnomAD rs777249439
- Missense
- Structural context available