ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
2
g.27079693G>T
CA1240107116
EMILIN1
c.171-458G>T (n.171-458G>T)
dbSNP
2
g.27079693G>A
CA11004743
EMILIN1
c.171-458G>A (n.171-458G>A)
dbSNP
gnomAD v2
gnomAD v3
gnomAD v4
Number of alleles fetched
Previous
Next