Canonical Allele Identifier: PA2827936895
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu355Pro
CA367399180
NM_001354800.1:c.1064T>C