Canonical Allele Identifier: PA2827936628
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804849
ClinVar RCV Id: RCV000992055 RCV001248939 RCV004017770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala188Thr
CA4239604
NM_001354800.1:c.562G>A