ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA096222
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.217370889
Linked Data - NCBI & NCI
ClinVar Allele:
259865
ClinVar RCV:
RCV000255753
RCV000763583
RCV003493556
RCV003987481
RCV004547644
ClinVar Variation:
265175
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Glu256Lys
CA4239527
NM_000162.5:c.766G>A