Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38551504C>TCA018670SCN5Ac.4865G>A (p.Arg1622Gln)
c.4868G>A (p.Arg1623Gln)
c.4814G>A (p.Arg1605Gln)
c.4706G>A (p.Arg1569Gln)
c.4769G>A (p.Arg1590Gln)
c.4739G>A (p.Arg1580Gln)
c.4811G>A (p.Arg1604Gln)
ClinVar dbSNP
3g.38551504C>ACA018677SCN5Ac.4865G>T (p.Arg1622Leu)
c.4868G>T (p.Arg1623Leu)
c.4814G>T (p.Arg1605Leu)
c.4706G>T (p.Arg1569Leu)
c.4769G>T (p.Arg1590Leu)
c.4739G>T (p.Arg1580Leu)
c.4811G>T (p.Arg1604Leu)
ClinVar dbSNP

Number of alleles fetched