| Approved symbol | H19 |
|---|---|
| Approved name | H19 imprinted maternally expressed transcript |
| HGCN ID | HGNC:4713 |
| Previous symbols | |
| Inheritance | |
| OMIM | 103280 |
| Chromosome | 11p15.5 |
| Panel(s) |
Methylering Chr.11p15 (KCNQ1OT1 & H19) Multi Locus Imprinting Disorders (MLID) NGS Mendelioom NGS Skeletdysplasie |
