Canonical Allele Identifier: PA2579982156
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 987827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg345Gly
CA367399354
NM_000162.5:c.1033C>G