ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
20
g.3083022C>A
CA121955
AVP
c.277G>T (p.Gly93Trp)
ClinVar
dbSNP
gnomAD v4
20
g.3083022C>T
CA408061561
AVP
c.277G>A (p.Gly93Arg)
dbSNP
gnomAD v4
Number of alleles fetched
Previous
Next