Canonical Allele Identifier: PA2827936792
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 992217
ClinVar RCV Id: RCV001280588 RCV002463801 RCV003481051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu271del
CA1703634895
NM_001354800.1:c.811_813del