Canonical Allele Identifier: PA2830123512
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1678597
ClinVar RCV Id: RCV002225198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met250Val
CA367400634
NM_033508.3:c.748A>G