W41L (p.Trp41Leu) variant of NF2 (Merlin)
W41L (p.Trp41Leu) in NF2 (Merlin) is a missense change. Clinical records from EBI and UniProt describe it as pathogenic. The record also includes structural context.
W41L (p.Trp41Leu) variant details
- p.Trp41Leu
- Ensembl rs1555986860
- Pathogenic
- Missense
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available