E37G (p.Glu37Gly) variant of SMAD2 (SMAD family member 2)
E37G (p.Glu37Gly) in SMAD2 (SMAD family member 2) is a missense change. The record also includes structural context.
E37G (p.Glu37Gly) variant details
- p.Glu37Gly
- Ensembl rs2033450316
- Missense
- Structural context available