Canonical Allele Identifier: PA645460273
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu257Asp
CA213848
NM_033507.3:c.771G>C
CA367400599
NM_033507.3:c.771G>T