Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.166002588C>TCA284940SCN1Ac.4168G>A (p.Val1390Met)
c.4084G>A (p.Val1362Met)
c.4135G>A (p.Val1379Met)
n.176-13025C>T
c.4165G>A (p.Val1389Met)
c.4132G>A (p.Val1378Met)
c.4003-2812G>A (p.=)
n.4416G>A
c.4081G>A (p.Val1361Met)
c.1726G>A (p.Val576Met)
n.4604G>A
n.4618G>A
n.4590G>A
n.4084G>A (p.Val1362Met)
n.321G>A
ClinVar dbSNP
2g.166002588C>GCA303554SCN1Ac.4168G>C (p.Val1390Leu)
c.4084G>C (p.Val1362Leu)
c.4135G>C (p.Val1379Leu)
n.176-13025C>G
c.4165G>C (p.Val1389Leu)
c.4132G>C (p.Val1378Leu)
c.4003-2812G>C (p.=)
n.4416G>C
c.4081G>C (p.Val1361Leu)
c.1726G>C (p.Val576Leu)
n.4604G>C
n.4618G>C
n.4590G>C
n.4084G>C (p.Val1362Leu)
n.321G>C
ClinVar dbSNP

Number of alleles fetched