Canonical Allele Identifier: PA2579978698
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile159Val
CA367401860
NM_000162.5:c.475A>G