Canonical Allele Identifier: PA2827937249
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Val118Glu
CA4239373
NM_001354801.1:c.353T>A