D162H (p.Asp162His) variant of CHM (P24386)
D162H (p.Asp162His) in CHM (P24386) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
D162H (p.Asp162His) variant details
- p.Asp162His
- ExAC rs755873471
- TOPMed rs755873471
- gnomAD rs755873471
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available