F47I (p.Phe47Ile) variant of MEN1 (Menin)
F47I (p.Phe47Ile) in MEN1 (Menin) is a missense change. The record also includes structural context.
F47I (p.Phe47Ile) variant details
- p.Phe47Ile
- cosmic curated COSV56345
- Missense
- Structural context available