Canonical Allele Identifier: PA2827936637
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804850
ClinVar RCV Id: RCV000992056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg191Gly
CA367401531
NM_001354800.1:c.571C>G