Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.132921437C>TCA007993TSC1c.664-1G>A (p.=)
c.511-1G>A (p.=)
c.301-1G>A (p.=)
n.860-1G>A
ClinVar dbSNP
9g.132921437C>GCA007999TSC1c.664-1G>C (p.=)
c.511-1G>C (p.=)
c.301-1G>C (p.=)
n.860-1G>C
ClinVar dbSNP

Number of alleles fetched