H13L (p.His13Leu) variant of GATA2 (P23769)
H13L (p.His13Leu) in GATA2 (P23769) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H13L (p.His13Leu) variant details
- p.His13Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available