S26C (p.Ser26Cys) variant of CPT2 (P23786)
S26C (p.Ser26Cys) in CPT2 (P23786) is a missense change. The record also includes structural context.
S26C (p.Ser26Cys) variant details
- p.Ser26Cys
- TOPMed rs1329746613
- gnomAD rs1329746613
- Missense
- Structural context available