Canonical Allele Identifier: PA2827936964
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995101
ClinVar RCV Id: RCV001288974 RCV002322180 RCV003446686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly388Asp
CA367398670
NM_001354800.1:c.1163G>A