Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.89178569G>ACA227574TYRc.616G>A (p.Ala206Thr)
n.677G>A
n.2718-65036C>T
n.2733-65036C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.89178569G=CA1989920905TYRc.616G= (p.Ala206=)
n.677G=
n.2718-65036C=
n.2733-65036C=
 dbSNP

Number of alleles fetched