G2Cdb::Allele report
- Mutation type
- MI
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 |
Literature (1)
Pubmed - other