Canonical Allele Identifier: PA2830122415
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg423Trp
CA367397271
NM_033507.3:c.1267C>T