S26T (p.Ser26Thr) variant of CPT2 (P23786)
S26T (p.Ser26Thr) in CPT2 (P23786) is a missense change. The record also includes structural context.
S26T (p.Ser26Thr) variant details
- p.Ser26Thr
- TOPMed rs1645327245
- Missense
- Structural context available
S26T (p.Ser26Thr) in CPT2 (P23786) is a missense change. The record also includes structural context.