Canonical Allele Identifier: PA1139748663
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995099
ClinVar RCV Id: RCV001288972 RCV002227265 RCV002464439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Lys40del
CA1139660059
NM_033507.3:c.118_120del