W41S (p.Trp41Ser) variant of NF2 (Merlin)
W41S (p.Trp41Ser) in NF2 (Merlin) is a missense change. Clinical records from EBI and UniProt describe it as pathogenic. The record also includes structural context.
W41S (p.Trp41Ser) variant details
- p.Trp41Ser
- Ensembl rs1555986860
- Pathogenic
- Missense
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available