Canonical Allele Identifier: PA2579975351
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664366
ClinVar RCV Id: RCV003445464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr326Pro
CA367399833
NM_000162.5:c.976A>C