Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.56565362C>TCA259705UBQLN2c.1489C>T (p.Pro497Ser)
c.273+1622C>T (n.273+1622C>T)
 ClinVar dbSNP
Xg.56565362C=CA2431031070UBQLN2c.1489C= (p.Pro497=)
c.273+1622C= (n.273+1622C=)
 dbSNP

Number of alleles fetched