Canonical Allele Identifier: PA2827937278
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ile10Asn
CA213729
NM_001354802.1:c.29T>A