Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.111410133C>GCA171902DCXc.266G>C (p.Arg89Pro)
c.509G>C (p.Arg170Pro)
c.484G>C
n.506G>C
 ClinVar dbSNP
Xg.111410133C>TCA414246760DCXc.266G>A (p.Arg89Gln)
c.509G>A (p.Arg170Gln)
c.484G>A
n.506G>A
 ClinVar dbSNP COSMIC COSMIC

Number of alleles fetched