Canonical Allele Identifier: PA2827936860
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36267
ClinVar RCV Id: RCV000029930 RCV002463616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe316Tyr
CA213868
NM_001354800.1:c.947T>A