Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904518C>ACA255176F8c.5593G>T (p.Asp1865Tyr)
c.5488G>T (p.Asp1830Tyr)
ClinVar dbSNP COSMIC COSMIC
Xg.154904518C>TCA255175F8c.5593G>A (p.Asp1865Asn)
c.5488G>A (p.Asp1830Asn)
ClinVar dbSNP

Number of alleles fetched