Canonical Allele Identifier: PA2579976240
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801683
ClinVar RCV Id: RCV002463842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser375Thr
CA367398856
NM_000162.5:c.1123T>A