Canonical Allele Identifier: PA2827936950
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024418
ClinVar RCV Id: RCV003883454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser383Trp
CA367398735
NM_001354800.1:c.1148C>G