Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.123427951G>CCA151420GRIA3c.1888G>C (p.Gly630Arg)
n.5217+9299C>G
 ClinVar dbSNP
Xg.123427951G>ACA414259524GRIA3c.1888G>A (p.Gly630Arg)
n.5217+9299C>T
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC

Number of alleles fetched