G52A (p.Gly52Ala) variant of NPC2 (P61916)
G52A (p.Gly52Ala) in NPC2 (P61916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G52A (p.Gly52Ala) variant details
- p.Gly52Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available