Canonical Allele Identifier: PA916050372
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu356Pro
CA367399180
NM_033507.3:c.1067T>C