Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38556460A>GCA018241SCN5Ac.4415T>C (p.Phe1472Ser)
c.4418T>C (p.Phe1473Ser)
c.4364T>C (p.Phe1455Ser)
c.4256T>C (p.Phe1419Ser)
c.4289T>C (p.Phe1430Ser)
c.4361T>C (p.Phe1454Ser)
ClinVar dbSNP
3g.38556460A>CCA018247SCN5Ac.4415T>G (p.Phe1472Cys)
c.4418T>G (p.Phe1473Cys)
c.4364T>G (p.Phe1455Cys)
c.4256T>G (p.Phe1419Cys)
c.4289T>G (p.Phe1430Cys)
c.4361T>G (p.Phe1454Cys)
ClinVar dbSNP

Number of alleles fetched