P28H (p.Pro28His) variant of MYLK (Q15746)
P28H (p.Pro28His) in MYLK (Q15746) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P28H (p.Pro28His) variant details
- p.Pro28His
- ESP rs141974889
- ExAC rs141974889
- TOPMed rs141974889
- gnomAD rs141974889
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available