Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
15	g.55223902C>G	CA117892	RAB27A	n.2490G>C c.454G>C (p.Ala152Pro) n.2622G>C	ClinVar dbSNP
15	g.55223902C>T	CA392529511	RAB27A	n.2490G>A c.454G>A (p.Ala152Thr) n.2622G>A	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched