W13R (p.Trp13Arg) variant of CD79B (P40259)
W13R (p.Trp13Arg) in CD79B (P40259) is a missense change. The record also includes structural context.
W13R (p.Trp13Arg) variant details
- p.Trp13Arg
- gnomAD rs1266437430
- Missense
- Structural context available
W13R (p.Trp13Arg) in CD79B (P40259) is a missense change. The record also includes structural context.