Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.48446701C>ACA016073FBN1c.5788+5G>T (p.=)
c.*1551+5G>T (p.=)
n.1095+5G>T
ClinVar dbSNP
15g.48446701C>TCA016065FBN1c.5788+5G>A (p.=)
c.*1551+5G>A (p.=)
n.1095+5G>A
ClinVar dbSNP gnomAD

Number of alleles fetched