G38A (p.Gly38Ala) variant of TSC1 (Hamartin)
G38A (p.Gly38Ala) in TSC1 (Hamartin) is a missense change. The record also includes structural context.
G38A (p.Gly38Ala) variant details
- p.Gly38Ala
- Ensembl rs2132271039
- Missense
- Structural context available