| Approved symbol | CCT2 |
|---|---|
| Approved name | chaperonin containing TCP1 subunit 2 |
| HGCN ID | HGNC:1615 |
| Previous symbols | |
| Inheritance | |
| OMIM | 605139 |
| Chromosome | 12q15 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
