Canonical Allele Identifier: PA2827936450
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg63Cys
CA4239707
NM_001354800.1:c.187C>T