Canonical Allele Identifier: PA2827936765
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu256Asp
CA213848
NM_001354800.1:c.768G>C
CA367400599
NM_001354800.1:c.768G>T