ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
17
g.43758681C>T
CA129828
SOST
c.61G>A (p.Val21Met)
ClinVar
dbSNP
17
g.43758681C>A
CA399703409
SOST
c.61G>T (p.Val21Leu)
ClinVar
dbSNP
Number of alleles fetched
Previous
Next