G58D (p.Gly58Asp) variant of MYLK (Q15746)
G58D (p.Gly58Asp) in MYLK (Q15746) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G58D (p.Gly58Asp) variant details
- p.Gly58Asp
- TOPMed rs1161966043
- gnomAD rs1161966043
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available