Canonical Allele Identifier: PA658668966
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp161Asn
CA367401849
NM_033507.3:c.481G>A