| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CAPN3, LOC126862115 (S154T) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | CAPN3, LOC126862115 (I156T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene