Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38557232C>ACA018099SCN5Ac.4295G>T (p.Gly1432Val)
c.4298G>T (p.Gly1433Val)
c.4246-654G>T (n.4246-654G>T)
c.4136G>T (p.Gly1379Val)
c.4169G>T (p.Gly1390Val)
c.4243-654G>T (n.4243-654G>T)
ClinVar dbSNP
3g.38557232C>TCA72943604SCN5Ac.4295G>A (p.Gly1432Glu)
c.4298G>A (p.Gly1433Glu)
c.4246-654G>A (n.4246-654G>A)
c.4136G>A (p.Gly1379Glu)
c.4169G>A (p.Gly1390Glu)
c.4243-654G>A (n.4243-654G>A)
dbSNP

Number of alleles fetched