LMNA c.992G>A 48098
| Gene: | LMNA |
|---|---|
| Coding Change (c.): | c.992G>A |
| Protein Change (p.): | p.Arg331Gln |
| ClinVar Name: | NM_170707.4(LMNA):c.992G>A (p.Arg331Gln) |
| ClinVar Number: | 48098 |
| Variant Forum: | Laminopathies Support Group |
| Gene: | LMNA |
|---|---|
| Coding Change (c.): | c.992G>A |
| Protein Change (p.): | p.Arg331Gln |
| ClinVar Name: | NM_170707.4(LMNA):c.992G>A (p.Arg331Gln) |
| ClinVar Number: | 48098 |
| Variant Forum: | Laminopathies Support Group |