Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122257347C>TCA119485CASRc.452C>T (p.Thr151Met)
n.371C>T
n.311C>T
c.9+2973C>T (n.9+2973C>T)
ClinVar dbSNP gnomAD v4
3g.122257347C=CA1397869888CASRc.452C= (p.Thr151=)
n.371C=
n.311C=
c.9+2973C= (n.9+2973C=)
dbSNP

Number of alleles fetched