Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.38446710G>CCA024799RYR1c.742G>C (p.Gly248Arg)
n.825G>C
n.742G>C (p.Gly248Arg)
ClinVar dbSNP ExAC gnomAD
19g.38446710G>TCA069619RYR1c.742G>T (p.Gly248Trp)
n.825G>T
n.742G>T (p.Gly248Trp)
dbSNP ExAC gnomAD
19g.38446710G>ACA024797RYR1c.742G>A (p.Gly248Arg)
n.825G>A
n.742G>A (p.Gly248Arg)
ClinVar dbSNP COSMIC

Number of alleles fetched