Canonical Allele Identifier: PA2579976753
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1803244
ClinVar RCV Id: RCV002466914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe133Val
CA367402121
NM_000162.5:c.397T>G