Canonical Allele Identifier: PA2741997493
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574158
ClinVar RCV Id: RCV003318523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr169Pro
CA367401755
NM_033507.3:c.505A>C