Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.64758670C>ACA381111386PYGMc.278G>T (p.Gly93Val)
c.244-404G>T (n.244-404G>T)
ClinVar dbSNP
11g.64758670C=CA1978928558PYGMc.278G= (p.Gly93=)
c.244-404G= (n.244-404G=)
dbSNP

Number of alleles fetched