Canonical Allele Identifier: PA2827936718
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1756314
ClinVar RCV Id: RCV002362470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala232Asp
CA367400762
NM_001354800.1:c.695C>A