ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
19
g.35851340C>T
CA250221
NPHS1
c.319G>A (p.Ala107Thr)
ClinVar
dbSNP
ExAC
gnomAD v2
gnomAD v3
gnomAD v4
COSMIC
19
g.35851340C=
CA2333851783
NPHS1
c.319G= (p.Ala107=)
dbSNP
Number of alleles fetched
Previous
Next