Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.13865797C>ACA384053400GRIN2Bc.411+1G>T (n.411+1G>T)
ClinVar dbSNP
12g.13865797C>TCA16609333GRIN2Bc.411+1G>A (n.411+1G>A)
ClinVar dbSNP

Number of alleles fetched