Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209634506G>ACA16040705LAMB3c.505C>T (p.Gln169Ter)
c.373-1373C>T (n.373-1373C>T)
ClinVar dbSNP
1g.209634506G=CA2484302745LAMB3c.505C= (p.Gln169=)
c.373-1373C= (n.373-1373C=)
dbSNP

Number of alleles fetched