Canonical Allele Identifier: PA2830123806
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804833
ClinVar RCV Id: RCV000992035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser374Pro
CA367398853
NM_033508.3:c.1120T>C