Canonical Allele Identifier: PA2579978278
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2504386
ClinVar RCV Id: RCV003231847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu20Pro
CA367403809
NM_000162.5:c.59T>C