Canonical Allele Identifier: PA2827936580
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp160Asn
CA367401849
NM_001354800.1:c.478G>A