Canonical Allele Identifier: PA2827936673
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met210Lys
CA204367
NM_001354800.1:c.629T>A