Canonical Allele Identifier: PA658668942
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp125His
CA367402212
NM_033507.3:c.373G>C