Canonical Allele Identifier: PA2830123551
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 918070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly257Ser
CA367400589
NM_033508.3:c.769G>A