Canonical Allele Identifier: PA213823
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36240
ClinVar RCV Id: RCV000029903 RCV002371786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys220Tyr
CA213822
NM_000162.5:c.659G>A