Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.66870419C>ACA312908PCc.786G>T (p.Glu262Asp)
n.290-20354G>T
c.666G>T (p.Glu222Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.66870419C>TCA475375977PCc.786G>A (p.Glu262=)
n.290-20354G>A
c.666G>A (p.Glu222=)
ClinVar dbSNP gnomAD v4

Number of alleles fetched