Canonical Allele Identifier: PA916039365
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36198
ClinVar RCV Id: RCV000029861 RCV001288979 RCV002381268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg67Gly
CA213756
NM_001354802.1:c.199C>G