R33K (p.Arg33Lys) variant of RET (P07949)
R33K (p.Arg33Lys) in RET (P07949) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
R33K (p.Arg33Lys) variant details
- p.Arg33Lys
- Ensembl rs2132657164
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available