ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32340335C>T
CA023442
BRCA2
c.5980C>T (p.Gln1994Ter)
c.5611C>T (p.Gln1871Ter)
n.5980C>T
ClinVar
dbSNP
13
g.32340335C=
CA2082808804
BRCA2
c.5980C= (p.Gln1994=)
c.5611C= (p.Gln1871=)
n.5980C=
dbSNP
Number of alleles fetched
Previous
Next