Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.3083037C>A	CA408061590	AVP	c.262G>T (p.Gly88Cys)	ClinVar dbSNP gnomAD v4
20	g.3083037C>T	CA121946	AVP	c.262G>A (p.Gly88Ser)	ClinVar dbSNP gnomAD v4
20	g.3083037C=	CA2346405553	AVP	c.262G= (p.Gly88=)	dbSNP

Number of alleles fetched