Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38597949T>GCA015766SCN5Ac.2042A>C (p.His681Pro)
c.1913A>C (p.His638Pro)
 ClinVar dbSNP
3g.38597949T>CCA352144904SCN5Ac.2042A>G (p.His681Arg)
c.1913A>G (p.His638Arg)
 dbSNP gnomAD v4

Number of alleles fetched