Canonical Allele Identifier: PA658669051
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Trp258Arg
CA367400597
NM_033507.3:c.772T>C
CA367400598
NM_033507.3:c.772T>A