Canonical Allele Identifier: PA2741868013
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2698504
ClinVar RCV Id: RCV003551796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ser96_Thr100del
CA2697557239
NM_001354801.1:c.286_300del