Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38603888C>ACA015256SCN5Ac.1714G>T (p.Ala572Ser)
c.1585G>T (p.Ala529Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38603888C=CA1358584946SCN5Ac.1714G= (p.Ala572=)
c.1585G= (p.Ala529=)
dbSNP
3g.38603888C>TCA352146556SCN5Ac.1714G>A (p.Ala572Thr)
c.1585G>A (p.Ala529Thr)
ClinVar dbSNP gnomAD v4
3g.38603888C>GCA352146560SCN5Ac.1714G>C (p.Ala572Pro)
c.1585G>C (p.Ala529Pro)
dbSNP gnomAD v4

Number of alleles fetched