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, 8 - (AD)
10.7
8673105
MYL3 (3p21.3-p21.2)
Myosin light chain 3
* Cardiomopathy, hypertrophic, mid-ventricular chamber type - MYL3