Canonical Allele Identifier: PA916039377
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Cys49Trp
CA367398928
NM_001354803.2:c.147C>G