Canonical Allele Identifier: PA2830123538
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Glu255Asp
CA213848
NM_033508.3:c.765G>C
CA367400599
NM_033508.3:c.765G>T