P66H (p.Pro66His) variant of PPP2R5D (Q14738)
P66H (p.Pro66His) in PPP2R5D (Q14738) 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.
P66H (p.Pro66His) variant details
- p.Pro66His
- rs2532471802
- ClinGen CA364179666
- ClinVar RCV003064109
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available