Canonical Allele Identifier: PA2580490805
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1752729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met211dup
CA2580615881
NM_033507.3:c.633_635dup