Y102X variant of TNFRSF13B (O14836)
Y102X in TNFRSF13B (O14836) is a missense change. Clinical records describe it as [].
Y102X variant details
- rs774955611
- []
- Missense
Y102X in TNFRSF13B (O14836) is a missense change. Clinical records describe it as [].