Canonical Allele Identifier: PA916039404
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg75Leu
CA341587
NM_001354803.2:c.224G>T