Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.160136665T>CCA256629ATP1A2c.2659T>C (p.Trp887Arg)
c.1740T>C
n.2762T>C
 ClinVar dbSNP
1g.160136665T=CA1140495935ATP1A2c.2659T= (p.Trp887=)
c.1740T=
n.2762T=
 dbSNP

Number of alleles fetched