Canonical Allele Identifier: PA2827937037
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu430Pro
CA213749
NM_001354800.1:c.1289T>C