Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.111410223C>ACA121596DCXc.176G>T (p.Arg59Leu)
c.419G>T (p.Arg140Leu)
c.394G>T
n.416G>T
ClinVar dbSNP
Xg.111410223C>TCA171866DCXc.176G>A (p.Arg59His)
c.419G>A (p.Arg140His)
c.394G>A
n.416G>A
ClinVar dbSNP COSMIC

Number of alleles fetched