De novo missense variants in TRAF7 cause developmental delay, congenital anomalies, and dysmorphic features.
- Cited forFUNCTION, INVOLVEMENT IN CAFDADD, VARIANTS CAFDADD GLU-346; GLY-371; ALA-601 AND GLN-655, CHARACTERIZATION OF VARIANTS CAFDADD GLU-346; GLY-371; ALA-601 AND GLN-655
- CategoriesFunction, Sequences, Disease & Variants
- SourceUniProtKB reviewed (Swiss-Prot)