Canonical Allele Identifier: PA2827936672
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804852
ClinVar RCV Id: RCV000992058 RCV003117664 RCV003493767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met210Thr
CA367401300
NM_001354800.1:c.629T>C