Approved symbol | CNTN2 |
---|---|
Approved name | contactin 2 |
HGCN ID | HGNC:2172 |
Previous symbols | TAX, AXT |
Inheritance | |
OMIM | 190197 |
Chromosome | 1q32.1 |
Panel(s) |
NGS Epilepsie NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) |