Canonical Allele Identifier: PA2827936649
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3234002
ClinVar RCV Id: RCV004527578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met202Arg
CA367401376
NM_001354800.1:c.605T>G