Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.123326163C>T	CA202721	GRIA3	c.646C>T (p.Arg216Ter)	ClinVar dbSNP gnomAD v4
X	g.123326163C>A	CA335234211	GRIA3	c.646C>A (p.Arg216=)	dbSNP gnomAD v4

Number of alleles fetched