Canonical Allele Identifier: PA2580229354
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1734018
ClinVar RCV Id: RCV002348865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala62Thr
CA367398732
NM_001354803.2:c.184G>A