A61P (p.Ala61Pro) variant of MYH7 (Myosin-7)
A61P (p.Ala61Pro) in MYH7 (Myosin-7) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hypertrophic cardiomyopathy. The record also includes structural context.
A61P (p.Ala61Pro) variant details
- p.Ala61Pro
- rs2502322145
- ClinGen CA389053651
- ClinVar RCV003750067
- Uncertain significance
- Hypertrophic cardiomyopathy
- Missense
- ClinVar: Uncertain significance (Hypertrophic cardiomyopathy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available