T16M (p.Thr16Met) variant of TGFB2 (P61812)
T16M (p.Thr16Met) in TGFB2 (P61812) is a missense change. The record also includes structural context.
T16M (p.Thr16Met) variant details
- p.Thr16Met
- TOPMed rs1173342696
- Missense
- Structural context available
T16M (p.Thr16Met) in TGFB2 (P61812) is a missense change. The record also includes structural context.