Canonical Allele Identifier: PA2830123426
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Cys219Phe
CA367401193
NM_033508.3:c.656G>T