Canonical Allele Identifier: PA2827937173
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg60Leu
CA341587
NM_001354801.1:c.179G>T