C26G (p.Cys26Gly) variant of MET (P08581)
C26G (p.Cys26Gly) in MET (P08581) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
C26G (p.Cys26Gly) variant details
- p.Cys26Gly
- Ensembl rs2116579595
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available