Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.3084620C>T	CA121950	AVP	c.55G>A (p.Ala19Thr)	ClinVar dbSNP COSMIC
20	g.3084620C=	CA2346406186	AVP	c.55G= (p.Ala19=)	dbSNP
20	g.3084620C>A	CA408062717	AVP	c.55G>T (p.Ala19Ser)	dbSNP gnomAD v4

Number of alleles fetched