R42G (p.Arg42Gly) variant of ATP6V1B1 (P15313)
R42G (p.Arg42Gly) in ATP6V1B1 (P15313) is a missense change. The record also includes structural context.
R42G (p.Arg42Gly) variant details
- p.Arg42Gly
- Ensembl rs1680068412
- Missense
- Structural context available