Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38606034G>ACA16043398SCN5Ac.1255C>T (p.Gln419Ter)
c.1126C>T (p.Gln376Ter)
ClinVar dbSNP
3g.38606034G>CCA352148654SCN5Ac.1255C>G (p.Gln419Glu)
c.1126C>G (p.Gln376Glu)
ClinVar dbSNP

Number of alleles fetched