Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.49228048C>ACA412919632CACNA1Fc.1106G>T (p.Gly369Val)
c.911G>T (p.Gly304Val)
 dbSNP
Xg.49228048C>TCA255937CACNA1Fc.1106G>A (p.Gly369Asp)
c.911G>A (p.Gly304Asp)
 ClinVar dbSNP

Number of alleles fetched