Canonical Allele Identifier: PA2579983059
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 450644
ClinVar RCV Id: RCV000524090 RCV003403237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala176Glu
CA367401673
NM_000162.5:c.527C>A