Canonical Allele Identifier: PA2579974415
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val427Gly
CA367397199
NM_000162.5:c.1280T>G