R32W (p.Arg32Trp) variant of MYPN (Myopalladin)
R32W (p.Arg32Trp) in MYPN (Myopalladin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R32W (p.Arg32Trp) variant details
- p.Arg32Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available