Canonical Allele Identifier: PA213759
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36199
ClinVar RCV Id: RCV000029862 RCV004527304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala449Thr
CA213758
NM_000162.5:c.1345G>A