Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.3083156C>A	CA121948	AVP	c.143G>T (p.Gly48Val)	ClinVar dbSNP gnomAD v4
20	g.3083156C>G	CA408061849	AVP	c.143G>C (p.Gly48Ala)	dbSNP

Number of alleles fetched