Canonical Allele Identifier: PA2827936756
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val253Gly
CA213844
NM_001354800.1:c.758T>G