Canonical Allele Identifier: PA2827937050
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338523
ClinVar RCV Id: RCV001817894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu440Gly
CA367397030
NM_001354800.1:c.1319A>G