Canonical Allele Identifier: PA2830123707
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu314His
CA213866
NM_033508.3:c.941T>A