A101V (p.Ala101Val) variant of TNFRSF13B (O14836)
A101V (p.Ala101Val) in TNFRSF13B (O14836) is a missense change. The record also includes structural context.
A101V (p.Ala101Val) variant details
- p.Ala101Val
- TOPMed rs1310977376
- gnomAD rs1310977376
- Missense
- Structural context available