Canonical Allele Identifier: PA2579980562
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2754882
ClinVar RCV Id: RCV003564073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu177Asp
CA367401655
NM_000162.5:c.531A>C
CA367401656
NM_000162.5:c.531A>T