Canonical Allele Identifier: PA2827937344
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Val47Gly
CA367397199
NM_001354802.1:c.140T>G