Canonical Allele Identifier: PA2827936902
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972983
ClinVar RCV Id: RCV001249301 RCV001751510 RCV002463792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr362Ile
CA367399081
NM_001354800.1:c.1085C>T