Canonical Allele Identifier: PA2827937102
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2578347
ClinVar RCV Id: RCV003326073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Cys34Tyr
CA367398935
NM_001354801.1:c.101G>A