G2Cdb::Allele report
- Mutation type
- SNP
Altered genes (1)
| Gene | Symbol | Species | Description |
|---|---|---|---|
| G00002000 | MYO5A | Homo sapiens | myosin VA (heavy chain 12, myoxin) |
Diseases (1)
| Disease | Description | Nervous effect |
|---|---|---|
| D00000236 | Hypertrophic cardiomyopathy (familial) | N |