Canonical Allele Identifier: PA916039379
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Cys49Phe
CA152950
NM_001354803.2:c.146G>T