Canonical Allele Identifier: PA2827937390
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg100Trp
CA367397271
NM_001354803.2:c.298C>T