Canonical Allele Identifier: PA2579979158
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly295Ser
CA367400140
NM_000162.5:c.883G>A