Canonical Allele Identifier: PA658669082
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val278Gly
CA367400467
NM_033507.3:c.833T>G