Canonical Allele Identifier: PA2579978406
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu122Val
CA367402231
NM_000162.5:c.364C>G