Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.49951000A>C	CA127486	AQP2	c.170A>C (p.Gln57Pro)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12	g.49951000A=	CA2035390568	AQP2	c.170A= (p.Gln57=)	dbSNP

Number of alleles fetched