Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.15189004A>GCA340888NOTCH3c.1363T>C (p.Cys455Arg)
c.1360T>C (p.Cys454Arg)
ClinVar dbSNP
19g.15189004A>TCA404527578NOTCH3c.1363T>A (p.Cys455Ser)
c.1360T>A (p.Cys454Ser)
ClinVar dbSNP
19g.15189004A=CA2324748606NOTCH3c.1363T= (p.Cys455=)
c.1360T= (p.Cys454=)
dbSNP

Number of alleles fetched