| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | ACTA1-related myopathies +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Familial restrictive cardiomyopathy +5 more | |
Click to view in NCBI Gene