Canonical Allele Identifier: PA2741868039
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024419
ClinVar RCV Id: RCV003883455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ser61Thr
CA367398738
NM_001354803.2:c.181T>A