Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.240877633G>T	CA275801	AGXT	c.942+1G>T (n.942+1G>T) n.720+1G>T	ClinVar dbSNP
2	g.240877633G>A	CA351319407	AGXT	c.942+1G>A (n.942+1G>A) n.720+1G>A	ClinVar dbSNP gnomAD v4

Number of alleles fetched