Canonical Allele Identifier: PA2827937144
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Leu49Val
CA367398705
NM_001354801.1:c.145C>G