Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.149482891A>TCA220492IDSc.1508T>A (p.Val503Asp)
c.875T>A (p.Val292Asp)
c.1238T>A (p.Val413Asp)
 ClinVar dbSNP
Xg.149482891A=CA2465003961IDSc.1508T= (p.Val503=)
c.875T= (p.Val292=)
c.1238T= (p.Val413=)
 dbSNP

Number of alleles fetched