CHEK2 c.1427C>T 128060
| Gene: | CHEK2 |
|---|---|
| Coding Change (c.): | c.1427C>T |
| Protein Change (p.): | p.Thr476Met |
| ClinVar Name: | NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met) |
| ClinVar Number: | 128060 |
| Variant Forum: | FORCE Share Your Mutation Message Board |
| Gene: | CHEK2 |
|---|---|
| Coding Change (c.): | c.1427C>T |
| Protein Change (p.): | p.Thr476Met |
| ClinVar Name: | NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met) |
| ClinVar Number: | 128060 |
| Variant Forum: | FORCE Share Your Mutation Message Board |