Canonical Allele Identifier: PA1139748832
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 976272
ClinVar RCV Id: RCV001253516 RCV002463794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu178Leu
CA1139660058
NM_033507.3:c.532_533delinsTT