Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.71570848A>TCA16609568CDH23c.683A>T (p.Asp228Val)
c.54A>T
n.459A>T
c.347A>T (p.Asp116Val)
c.698A>T (p.Asp233Val)
c.461+3A>T (n.461+3A>T)
c.818A>T (p.Asp273Val)
c.278A>T (p.Asp93Val)
n.162-5714T>A
n.1061A>T
ClinVar dbSNP
10g.71570848A=CA1918769700CDH23c.683A= (p.Asp228=)
c.54A=
n.459A=
c.347A= (p.Asp116=)
c.698A= (p.Asp233=)
c.461+3A= (n.461+3A=)
c.818A= (p.Asp273=)
c.278A= (p.Asp93=)
n.162-5714T=
n.1061A=
dbSNP

Number of alleles fetched