Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38606090C>GCA014496SCN5Ac.1199G>C (p.Gly400Ala)
c.1070G>C (p.Gly357Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38606090C>TCA352148866SCN5Ac.1199G>A (p.Gly400Glu)
c.1070G>A (p.Gly357Glu)
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched