Chain636: Familial Hemiplegic Migraine 2
This is a rare disease.
Example use A
Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.
Developer
Dr. Colby
Genetic info
Genes | Genetic variants |
---|---|
ATP1A2 | chr1:160105036,chr1:160105300 |