Canonical Allele Identifier: PA2579977462
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2110197
ClinVar RCV Id: RCV003042239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Lys190Glu
CA367401542
NM_000162.5:c.568A>G