Canonical Allele Identifier: PA2825042519
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala454dup
CA645372837
NM_000162.5:c.1361_1363dup