A49T (p.Ala49Thr) variant of MYD88 (Q99836)
A49T (p.Ala49Thr) in MYD88 (Q99836) is a missense change. The record also includes structural context.
A49T (p.Ala49Thr) variant details
- p.Ala49Thr
- gnomAD rs1700995743
- Missense
- Structural context available
A49T (p.Ala49Thr) in MYD88 (Q99836) is a missense change. The record also includes structural context.