Canonical Allele Identifier: PA2579976881
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679548
ClinVar RCV Id: RCV002227427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe438Val
CA367397071
NM_000162.5:c.1312T>G