Canonical Allele Identifier: PA2827937353
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ile56Asn
CA213751
NM_001354802.1:c.167T>A