Canonical Allele Identifier: PA2827936606
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136524
ClinVar RCV Id: RCV003037220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala176Thr
CA367401678
NM_001354800.1:c.526G>A