Canonical Allele Identifier: PA2827937166
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_001341730.1:p.Arg57Cys
CA367398588
NM_001354801.1:c.169C>T