BRCA2 c.7878G>C 38125
| Gene: | BRCA2 |
|---|---|
| Coding Change (c.): | c.7878G>C |
| Protein Change (p.): | p.Trp2626Cys |
| ClinVar Name: | NM_000059.4(BRCA2):c.7878G>C (p.Trp2626Cys) |
| ClinVar Number: | 38125 |
| Variant Forum: | FORCE Share Your Mutation Message Board |
| Gene: | BRCA2 |
|---|---|
| Coding Change (c.): | c.7878G>C |
| Protein Change (p.): | p.Trp2626Cys |
| ClinVar Name: | NM_000059.4(BRCA2):c.7878G>C (p.Trp2626Cys) |
| ClinVar Number: | 38125 |
| Variant Forum: | FORCE Share Your Mutation Message Board |