Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.3083022C>A	CA121955	AVP	c.277G>T (p.Gly93Trp)	ClinVar dbSNP gnomAD v4
20	g.3083022C>T	CA408061561	AVP	c.277G>A (p.Gly93Arg)	dbSNP gnomAD v4
20	g.3083022C=	CA2346405542	AVP	c.277G= (p.Gly93=)	dbSNP

Number of alleles fetched