LMNA c.1556C>T 499025
| Gene: | LMNA |
|---|---|
| Coding Change (c.): | LMNA c.1556C>T |
| Protein Change (p.): | p.Thr519Ile |
| ClinVar Name: | NM_170707.4(LMNA):c.1556C>T (p.Thr519Ile) |
| ClinVar Number: | 499025 |
| Variant Forum: | Facebook Laminopathies Support Group |
| Gene: | LMNA |
|---|---|
| Coding Change (c.): | LMNA c.1556C>T |
| Protein Change (p.): | p.Thr519Ile |
| ClinVar Name: | NM_170707.4(LMNA):c.1556C>T (p.Thr519Ile) |
| ClinVar Number: | 499025 |
| Variant Forum: | Facebook Laminopathies Support Group |