D92H (p.Asp92His) variant of DDC (P20711)
D92H (p.Asp92His) in DDC (P20711) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D92H (p.Asp92His) variant details
- p.Asp92His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available