Gene table: search width pubmed_id = 7981753


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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, 2 - (AD)
10.2
7493025
7889574
7981753
8205619
8528244
TNNT2 (1q32)
Troponin T2, cardiac
* Cardiomyopathy, familial hypertrophic, 2 - CMH2
* Left ventricular noncompaction 6 - LVNC6
* Cardiomyopathy, dilated, 1D - CMD1D