Lynch Syndrome HNPCC Syndrome
| TEST CODE | MG00340 |
| TEST NAME | Lynch Syndrome HNPCC Syndrome |
| RELATED GENE | PMS1 |
| SYNONYMOUS | PMS1 |
| OMIM | 600258 |
| HEREDITY | |
| CLINICAL AREA | Lynch Syndrome HNPCC Syndrome is an autosomal dominantly inherited disease. Mutations in the PMS1 gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA / CVS |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
ORDER OPTIONS AND PRICING
Discover genetic insights at your convenience. Contact Mikrogen anytime for information on order options, pricing, and comprehensive genetic testing services


