P6T (p.Pro6Thr) variant of MYD88 (Q99836)
P6T (p.Pro6Thr) in MYD88 (Q99836) is a missense change. The record also includes structural context.
P6T (p.Pro6Thr) variant details
- p.Pro6Thr
- TOPMed rs1300885784
- gnomAD rs1300885784
- Missense
- Structural context available