Canonical Allele Identifier: PA2579979170
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233734
ClinVar RCV Id: RCV004526584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly285Val
CA367400418
NM_000162.5:c.854G>T