Canonical Allele Identifier: PA2827937190
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801514
ClinVar RCV Id: RCV002463834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Gly73Val
CA367398308
NM_001354801.1:c.218G>T