A26G (p.Ala26Gly) variant of RET (P07949)
A26G (p.Ala26Gly) in RET (P07949) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A26G (p.Ala26Gly) variant details
- p.Ala26Gly
- Ensembl rs2132656365
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available