Canonical Allele Identifier: PA2827936903
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 418228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp363Asn
CA16618466
NM_001354800.1:c.1087G>A