Research Article

Genetic Diversity of SCN5A Gene and Its Possible Association with the Concealed Form of Brugada Syndrome Development in Polish Group of Patients

Figure 3

Sequence alignment of SCN5 exon 2 reference (WT) and MT amplicon detected in sample 5 (pos. 38614716 heterozygote A>G, exon, amino acid pos. 29, polymorphism rs6599230; pos. 38614815 heterozygote G>C, exon, pos. 182 in mRNA, nontraslanted region). White color shows changed nucleotides.