Canonical Allele Identifier: PA645460213
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36237
ClinVar RCV Id: RCV000029900 RCV000482920 RCV002287347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser213del
CA213816
NM_033507.3:c.638_640del