Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.166228971A>TCA118143SCN1A-AS1,SCN9Ac.3926T>A (p.Val1309Asp)
c.3770T>A (p.Val1257Asp)
c.3893T>A (p.Val1298Asp)
n.612-19224A>T
c.3539T>A (p.Val1180Asp)
c.3182T>A (p.Val1061Asp)
ClinVar dbSNP
2g.166228971A=CA1304943724SCN1A-AS1,SCN9Ac.3926T= (p.Val1309=)
c.3770T= (p.Val1257=)
c.3893T= (p.Val1298=)
n.612-19224A=
c.3539T= (p.Val1180=)
c.3182T= (p.Val1061=)
dbSNP

Number of alleles fetched