Canonical Allele Identifier: PA645460208
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met211Lys
CA204367
NM_033507.3:c.632T>A