Canonical Allele Identifier: PA2830123211
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338246
ClinVar RCV Id: RCV001822844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe170Val
CA367401725
NM_033508.3:c.508T>G