Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.48537809C>ACA10603465FBN1c.539-1G>T (n.539-1G>T)
ClinVar dbSNP
15g.48537809C>TCA015791FBN1c.539-1G>A (n.539-1G>A)
ClinVar dbSNP

Number of alleles fetched