Canonical Allele Identifier: PA916039376
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 381598
ClinVar RCV Id: RCV000440624 RCV003325955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val45Met
CA16605802
NM_001354803.2:c.133G>A