Canonical Allele Identifier: PA2830122848
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1803833
ClinVar RCV Id: RCV002468458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Glu92Ala
CA367402868
NM_033508.3:c.275A>C