Canonical Allele Identifier: PA645460334
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu316His
CA213866
NM_033507.3:c.947T>A