Canonical Allele Identifier: PA2827937401
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_001341732.1:p.Ser111_Thr115del
CA2697557239
NM_001354803.2:c.331_345del