Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.215420652T>CCA2095210FN1c.1675+21A>G (n.1675+21A>G)
n.598+21A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.215420652T>ACA1327366901FN1c.1675+21A>T (n.1675+21A>T)
n.598+21A>T
dbSNP

Number of alleles fetched