Canonical Allele Identifier: PA2827937151
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_001341730.1:p.Gly51Asp
CA367398670
NM_001354801.1:c.152G>A