Canonical Allele Identifier: PA213750
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu430Pro
CA213749
NM_000162.5:c.1289T>C