Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.3083005G>T	CA121952	AVP	c.294C>A (p.Cys98Ter)	ClinVar dbSNP gnomAD v4
20	g.3083005G>A	CA9739443	AVP	c.294C>T (p.Cys98=)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched