Canonical Allele Identifier: PA2827937396
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val105Gly
CA367397199
NM_001354803.2:c.314T>G