Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.165992332C>ACA317561SCN1Ac.4943G>T (p.Arg1648Leu)
c.4859G>T (p.Arg1620Leu)
c.4910G>T (p.Arg1637Leu)
n.176-23281C>A
c.4940G>T (p.Arg1647Leu)
c.4907G>T (p.Arg1636Leu)
c.4661G>T (p.Arg1554Leu)
c.4856G>T (p.Arg1619Leu)
c.2501G>T (p.Arg834Leu)
n.5379G>T
n.5393G>T
n.5365G>T
n.4859G>T (p.Arg1620Leu)
ClinVar dbSNP
2g.165992332C>TCA256584SCN1Ac.4943G>A (p.Arg1648His)
c.4859G>A (p.Arg1620His)
c.4910G>A (p.Arg1637His)
n.176-23281C>T
c.4940G>A (p.Arg1647His)
c.4907G>A (p.Arg1636His)
c.4661G>A (p.Arg1554His)
c.4856G>A (p.Arg1619His)
c.2501G>A (p.Arg834His)
n.5379G>A
n.5393G>A
n.5365G>A
n.4859G>A (p.Arg1620His)
ClinVar dbSNP

Number of alleles fetched