Canonical Allele Identifier: PA658669153
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe420Leu
CA367397305
NM_033507.3:c.1260C>G
CA367397306
NM_033507.3:c.1260C>A
CA367397316
NM_033507.3:c.1258T>C