Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.48516364T>CCA011982FBN1c.1148-2A>G (n.1148-2A>G)
c.636+21347A>G (n.636+21347A>G)
ClinVar dbSNP
15g.48516364T>GCA011972FBN1c.1148-2A>C (n.1148-2A>C)
c.636+21347A>C (n.636+21347A>C)
ClinVar dbSNP

Number of alleles fetched