Canonical Allele Identifier: PA2499252080
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256313
ClinVar RCV Id: RCV001663655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val84dup
CA2499218894
NM_001354803.2:c.251_253dup