Canonical Allele Identifier: PA2830123877
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233999
ClinVar RCV Id: RCV004527575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu385Arg
CA367398699
NM_033508.3:c.1154T>G