L41V (p.Leu41Val) variant of MEN1 (Menin)
L41V (p.Leu41Val) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
L41V (p.Leu41Val) variant details
- p.Leu41Val
- TOPMed rs1441672096
- gnomAD rs1441672096
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available