Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.94001000G>CCA227400ABCA4c.6386+2C>G (n.6386+2C>G)
c.2762+2C>G (n.2762+2C>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.94001000G=CA1140725971ABCA4c.6386+2C= (n.6386+2C=)
c.2762+2C= (n.2762+2C=)
dbSNP

Number of alleles fetched