Canonical Allele Identifier: PA2579977768
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu355Pro
CA367399180
NM_000162.5:c.1064T>C