Canonical Allele Identifier: PA2827936419
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585913
ClinVar RCV Id: RCV000711764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg43Pro
CA367403448
NM_001354800.1:c.128G>C