Canonical Allele Identifier: PA2741868028
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2775417
ClinVar RCV Id: RCV003577094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ser38Leu
CA367399114
NM_001354803.2:c.113C>T