Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.7267518C>TCA124238INSRc.479G>A (p.Trp160Ter)
n.454G>A
c.557G>A (p.Trp186Ter)
 ClinVar dbSNP gnomAD v4
19g.7267518C=CA2320836444INSRc.479G= (p.Trp160=)
n.454G=
c.557G= (p.Trp186=)
 dbSNP

Number of alleles fetched