Approved symbol | TSC2 |
---|---|
Approved name | TSC complex subunit 2 |
HGCN ID | HGNC:12363 |
Previous symbols | TSC4 |
Inheritance | |
OMIM | 191092 |
Chromosome | 16p13.3 |
Panel(s) |
NGS Epilepsie NGS Intellectual disability NGS Lymfoedeem NGS Mendelioom NGS Niercelcarcinoom NGS Oncopanel 1 NGS Oncopanel 2 NGS Polyposis NGS Segmentale overgroei en Vasculaire malformaties (somatisch) |