Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.2445099A>G	CA006661	KCNQ1	c.24-284A>G (n.24-284A>G) c.1A>G (p.Met1Val)	ClinVar dbSNP gnomAD v4
11	g.2445099A>T	CA350383	KCNQ1	c.24-284A>T (n.24-284A>T) c.1A>T (p.Met1Leu)	ClinVar dbSNP gnomAD v4

Number of alleles fetched