Canonical Allele Identifier: PA2580229279
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.His87Tyr
CA367397245
NM_001354801.1:c.259C>T