V40G (p.Val40Gly) variant of MEN1 (Menin)
V40G (p.Val40Gly) in MEN1 (Menin) is a missense change. The record also includes structural context.
V40G (p.Val40Gly) variant details
- p.Val40Gly
- ExAC rs747617261
- gnomAD rs747617261
- Missense
- Structural context available