Canonical Allele Identifier: PA658669136
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala380Gly
CA367398793
NM_033507.3:c.1139C>G