Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.123465757G>TCA414266320GRIA3c.2324+645G>T (n.2324+645G>T)
c.2408G>T (p.Gly803Val)
n.4959+997C>A
ClinVar dbSNP
Xg.123465757G>ACA16609121GRIA3c.2324+645G>A (n.2324+645G>A)
c.2408G>A (p.Gly803Glu)
n.4959+997C>T
ClinVar dbSNP

Number of alleles fetched