Canonical Allele Identifier: PA2827937101
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Cys34Trp
CA367398928
NM_001354801.1:c.102C>G