Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38620901C>TCA019331SCN5Ac.553G>A (p.Ala185Thr)
n.748G>A
c.482+1499G>A (n.482+1499G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38620901C=CA1358592327SCN5Ac.553G= (p.Ala185=)
n.748G=
c.482+1499G= (n.482+1499G=)
dbSNP

Number of alleles fetched