Canonical Allele Identifier: PA2827936708
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_001341729.1:p.Thr228Ala
CA367400790
NM_001354800.1:c.682A>G