Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.38510566G>TCA024959RYR1c.9000+1G>T (p.=)
c.8997+1G>T (p.=)
n.9083+1G>T
n.9000+1G>T (p.=)
n.2452+1G>T
ClinVar dbSNP
19g.38510566G>ACA308123148RYR1c.9000+1G>A (p.=)
c.8997+1G>A (p.=)
n.9083+1G>A
n.9000+1G>A (p.=)
n.2452+1G>A
dbSNP

Number of alleles fetched