Canonical Allele Identifier: PA2830123399
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1752729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met209dup
CA2580615881
NM_033508.3:c.627_629dup