Canonical Allele Identifier: PA096376
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 997861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu164Pro
CA367401792
NM_000162.5:c.491T>C