Canonical Allele Identifier: PA645461094
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg448Gln
CA367396940
NM_033507.3:c.1343G>A