Canonical Allele Identifier: PA2741868050
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2571660
ClinVar RCV Id: RCV003313370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Phe97Val
CA367397313
NM_001354803.2:c.289T>G