Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38550324C>TCA16609848SCN5Ac.6045G>A (p.Val2015=)
c.6048G>A (p.Val2016=)
c.5994G>A (p.Val1998=)
c.5886G>A (p.Val1962=)
c.5949G>A (p.Val1983=)
c.5919G>A (p.Val1973=)
c.5991G>A (p.Val1997=)
ClinVar dbSNP
3g.38550324C=CA1358561697SCN5Ac.6045G= (p.Val2015=)
c.6048G= (p.Val2016=)
c.5994G= (p.Val1998=)
c.5886G= (p.Val1962=)
c.5949G= (p.Val1983=)
c.5919G= (p.Val1973=)
c.5991G= (p.Val1997=)
dbSNP

Number of alleles fetched