S123A (p.Ser123Ala) variant of HMGCS2 (P54868)
S123A (p.Ser123Ala) in HMGCS2 (P54868) is a missense change. The record also includes structural context.
S123A (p.Ser123Ala) variant details
- p.Ser123Ala
- TOPMed rs1300010645
- gnomAD rs1300010645
- Missense
- Structural context available