Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904493G>CCA255178F8c.5618C>G (p.Pro1873Arg)
c.5513C>G (p.Pro1838Arg)
 ClinVar dbSNP
Xg.154904493G>ACA414908172F8c.5618C>T (p.Pro1873Leu)
c.5513C>T (p.Pro1838Leu)
 dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched