Canonical Allele Identifier: PA2580229362
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1950859
ClinVar RCV Id: RCV002681549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg72Cys
CA367398588
NM_001354803.2:c.214C>T