Canonical Allele Identifier: PA2741997638
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735005
ClinVar RCV Id: RCV003555335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr256Ala
CA367400608
NM_033507.3:c.766A>G