Canonical Allele Identifier: PA2827937387
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1800884
ClinVar RCV Id: RCV002462481 RCV003418533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg100Leu
CA157911892
NM_001354803.2:c.299G>T