A49G (p.Ala49Gly) variant of MYD88 (Q99836)
A49G (p.Ala49Gly) in MYD88 (Q99836) is a missense change. The record also includes structural context.
A49G (p.Ala49Gly) variant details
- p.Ala49Gly
- TOPMed rs1156783898
- Missense
- Structural context available
A49G (p.Ala49Gly) in MYD88 (Q99836) is a missense change. The record also includes structural context.