T52A (p.Thr52Ala) variant of MYL2 (P10916)
T52A (p.Thr52Ala) in MYL2 (P10916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
T52A (p.Thr52Ala) variant details
- p.Thr52Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available