H91D (p.His91Asp) variant of MAOB (P27338)
H91D (p.His91Asp) in MAOB (P27338) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H91D (p.His91Asp) variant details
- p.His91Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available