Canonical Allele Identifier: PA2579975587
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1191898
ClinVar RCV Id: RCV001553149 RCV002271659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr206Met
CA367401337
NM_000162.5:c.617C>T