V56G (p.Val56Gly) variant of ADNP (Q9H2P0)
V56G (p.Val56Gly) in ADNP (Q9H2P0) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
V56G (p.Val56Gly) variant details
- p.Val56Gly
- rs2515616123
- ClinGen CA408981489
- ClinVar RCV003573818
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available