Canonical Allele Identifier: PA2830122366
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1879689
ClinVar RCV Id: RCV002512334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val413Leu
CA367398284
NM_033507.3:c.1237G>T
CA367398286
NM_033507.3:c.1237G>C