Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.101398906C>TCA021972GLA,RPL36A-HNRNPH2c.680G>A (p.Arg227Gln)
c.300+3449C>T (p.=)
c.177+7084C>T (p.=)
n.229G>A
n.518G>A
c.*68G>A (p.=)
c.408+3449C>T (p.=)
c.285+7084C>T (p.=)
n.765G>A
n.786G>A
ClinVar dbSNP
Xg.101398906C>GCA089014GLA,RPL36A-HNRNPH2c.680G>C (p.Arg227Pro)
c.300+3449C>G (p.=)
c.177+7084C>G (p.=)
n.229G>C
n.518G>C
c.*68G>C (p.=)
c.408+3449C>G (p.=)
c.285+7084C>G (p.=)
n.765G>C
n.786G>C
ClinVar dbSNP

Number of alleles fetched