Canonical Allele Identifier: PA2830123460
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447413
ClinVar RCV Id: RCV000516688 RCV001248971 RCV002367714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr227Ala
CA367400790
NM_033508.3:c.679A>G