Canonical Allele Identifier: PA2579977613
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807279
ClinVar RCV Id: RCV002475236 RCV003479431 RCV003493961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Lys56Thr
CA367403326
NM_000162.5:c.167A>C