H97Q (p.His97Gln) variant of MYLK (Q15746)
H97Q (p.His97Gln) in MYLK (Q15746) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H97Q (p.His97Gln) variant details
- p.His97Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available