Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38566555G>ACA017416SCN5Ac.3691C>T (p.Arg1231Trp)
c.3694C>T (p.Arg1232Trp)
c.3532C>T (p.Arg1178Trp)
c.3565C>T (p.Arg1189Trp)
ClinVar dbSNP gnomAD v4
3g.38566555G>CCA352149406SCN5Ac.3691C>G (p.Arg1231Gly)
c.3694C>G (p.Arg1232Gly)
c.3532C>G (p.Arg1178Gly)
c.3565C>G (p.Arg1189Gly)
dbSNP
3g.38566555G=CA1358569777SCN5Ac.3691C= (p.Arg1231=)
c.3694C= (p.Arg1232=)
c.3532C= (p.Arg1178=)
c.3565C= (p.Arg1189=)
dbSNP

Number of alleles fetched