Canonical Allele Identifier: PA2825078171
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256313
ClinVar RCV Id: RCV001663655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val406dup
CA2499218894
NM_000162.5:c.1217_1219dup