Canonical Allele Identifier: PA2830123967
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1879689
ClinVar RCV Id: RCV002512334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val411Leu
CA367398284
NM_033508.3:c.1231G>T
CA367398286
NM_033508.3:c.1231G>C