Canonical Allele Identifier: PA2830124025
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1769016
ClinVar RCV Id: RCV002383233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu429Val
CA367397172
NM_033508.3:c.1285C>G