Canonical Allele Identifier: PA2741868038
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024418
ClinVar RCV Id: RCV003883454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ser61Trp
CA367398735
NM_001354803.2:c.182C>G