Canonical Allele Identifier: PA2830123472
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1756314
ClinVar RCV Id: RCV002362470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala231Asp
CA367400762
NM_033508.3:c.692C>A