Canonical Allele Identifier: PA1139735194
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Thr5Pro
CA157913750
NM_001354801.1:c.13A>C