Approved symbol | LMNB2 |
---|---|
Approved name | lamin B2 |
HGCN ID | HGNC:6638 |
Previous symbols | LMN2 |
Inheritance | |
OMIM | 150341 |
Chromosome | 19p13.3 |
Panel(s) |
NGS Intellectual disability NGS Mendelioom NGS Metabole aandoeningen NGS Preconceptiepanel (t.b.v. consanguine paren) |