Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38620900G>ACA019348SCN5Ac.554C>T (p.Ala185Val)
n.749C>T
c.482+1500C>T (n.482+1500C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38620900G>TCA352153769SCN5Ac.554C>A (p.Ala185Glu)
n.749C>A
c.482+1500C>A (n.482+1500C>A)
dbSNP gnomAD v4

Number of alleles fetched