Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.155116561T>ACA10584008MMEc.439+2T>A (n.439+2T>A)
n.282+2T>A
ClinVar dbSNP gnomAD v4
3g.155116561T=CA1412787807MMEc.439+2T= (n.439+2T=)
n.282+2T=
dbSNP

Number of alleles fetched