ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2579982925
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.030119002
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000490143
RCV000754816
RCV002350083
RCV002496884
RCV003318499
ClinVar Variation:
426122
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Arg191Trp
CA367401530
NM_000162.5:c.571C>T