ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
17
g.41586438C>G
CA216939
KRT14
c.397G>C (p.Val133Leu)
ClinVar
dbSNP
17
g.41586438C>T
CA216937
KRT14
c.397G>A (p.Val133Met)
ClinVar
dbSNP
COSMIC
17
g.41586438C>A
CA216941
KRT14
c.397G>T (p.Val133Leu)
ClinVar
dbSNP
Number of alleles fetched
Previous
Next