Canonical Allele Identifier: PA2827936984
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg397Leu
CA341587
NM_001354800.1:c.1190G>T