Canonical Allele Identifier: PA2741997509
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664850
ClinVar RCV Id: RCV003447825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu186Pro
CA367401583
NM_033507.3:c.557T>C