Canonical Allele Identifier: PA2830122070
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908614
ClinVar Variation Id: 1338685
ClinVar RCV Id: RCV001818056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val375Leu
CA367398872
NM_033507.3:c.1123G>T
CA367398880
NM_033507.3:c.1123G>C