Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
3	g.10142124G>A	CA020230	VHL	c.277G>A (p.Gly93Ser)	ClinVar dbSNP gnomAD v4 COSMIC
3	g.10142124G>C	CA357130	VHL	c.277G>C (p.Gly93Arg)	ClinVar dbSNP COSMIC
3	g.10142124G>T	CA357106	VHL	c.277G>T (p.Gly93Cys)	ClinVar dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched