Canonical Allele Identifier: PA2830122999
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp123His
CA367402212
NM_033508.3:c.367G>C