ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579979585
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.282776345
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000502130
RCV000517681
RCV000763585
RCV002367690
RCV003403165
ClinVar Variation:
435306
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Gly223Ser
CA367401165
NM_000162.5:c.667G>A