Canonical Allele Identifier: PA2580229323
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1802685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val45Leu
CA367398995
NM_001354803.2:c.133G>T
CA367398997
NM_001354803.2:c.133G>C