A11G (p.Ala11Gly) variant of NRAS (GTPase NRas)
A11G (p.Ala11Gly) in NRAS (GTPase NRas) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of RASopathy. The record also includes structural context.
A11G (p.Ala11Gly) variant details
- p.Ala11Gly
- Ensembl rs2101744270
- Uncertain significance
- RASopathy
- Missense
- ClinVar: Uncertain significance (RASopathy)
- UniProt: Uncertain significance
- Structural context available