Canonical Allele Identifier: PA2827936783
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21078
ClinVar RCV Id: RCV000020168 RCV003398550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly264Ser
CA341589
NM_001354800.1:c.790G>A