Canonical Allele Identifier: PA213757
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_000153.1:p.Arg447Gly
CA213756
NM_000162.5:c.1339C>G