Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38606757C>TCA014239SCN5Ac.1052G>A (p.Gly351Asp)
c.923G>A (p.Gly308Asp)
 ClinVar dbSNP
3g.38606757C>ACA014246SCN5Ac.1052G>T (p.Gly351Val)
c.923G>T (p.Gly308Val)
 ClinVar dbSNP

Number of alleles fetched