Canonical Allele Identifier: PA2827936759
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asn254His
CA213846
NM_001354800.1:c.760A>C