Canonical Allele Identifier: PA2827936398
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972809
ClinVar RCV Id: RCV001249065 RCV001879749 RCV002464037 RCV002485984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg36Gln
CA367403564
NM_001354800.1:c.107G>A