Canonical Allele Identifier: PA096386
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338573
ClinVar RCV Id: RCV001817944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu309Pro
CA367400002
NM_000162.5:c.926T>C