Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.101504550G>TCA10581553TRPC6c.419C>A (p.Ala140Glu)
c.254C>A (p.Ala85Glu)
n.775C>A
ClinVar dbSNP
11g.101504550G=CA1995875021TRPC6c.419C= (p.Ala140=)
c.254C= (p.Ala85=)
n.775C=
dbSNP

Number of alleles fetched