Gene table: search width pubmed_id = 8673105


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Familial hypertrophic cardiomyopathy, 10 - (AD)
10.9
8673105
MYL2 (12q23-q24.3)
Myosin light chain 2
* myopathy, congenital, with fiber-type disproportion - CFTD
* Cardiomyopathy, familial hypertrophic, 10 - CMH10
* Cardiomyopathy, hypertrophic, 10 - CMH10