ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579979579
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.29549635
Linked Data - NCBI & NCI
ClinVar RCV:
RCV003060105
ClinVar Variation:
2136520
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Gly223Val
CA367401157
NM_000162.5:c.668G>T