Canonical Allele Identifier: PA2827936587
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 997861
ClinVar RCV Id: RCV001293474 RCV001871744 RCV003127763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu164Pro
CA367401792
NM_001354800.1:c.491T>C