Canonical Allele Identifier: PA2827936619
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129144
ClinVar RCV Id: RCV000117131 RCV000255191 RCV000763586 RCV001248908 RCV002345419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val182Met
CA152954
NM_001354800.1:c.544G>A