S66T (p.Ser66Thr) variant of PPARGC1A (Q9UBK2)
S66T (p.Ser66Thr) in PPARGC1A (Q9UBK2) is a missense change. The record also includes structural context.
S66T (p.Ser66Thr) variant details
- p.Ser66Thr
- TOPMed rs1017037521
- gnomAD rs1017037521
- Missense
- Structural context available