ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
1
g.209623693G>A
CA16040692
LAMB3
c.2170C>T (p.Gln724Ter)
c.1978C>T (p.Gln660Ter)
ClinVar
dbSNP
1
g.209623693G=
CA2484298337
LAMB3
c.2170C= (p.Gln724=)
c.1978C= (p.Gln660=)
dbSNP
Number of alleles fetched
Previous
Next