Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.48610808C>GCA013283FBN1c.266G>C (p.Cys89Ser)
ClinVar dbSNP
15g.48610808C>TCA013275FBN1c.266G>A (p.Cys89Tyr)
ClinVar dbSNP
15g.48610808C>ACA270059115FBN1c.266G>T (p.Cys89Phe)
ClinVar dbSNP
15g.48610808C=CA2175573540FBN1c.266G= (p.Cys89=)
dbSNP

Number of alleles fetched