Canonical Allele Identifier: PA2827937041
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile436Asn
CA213751
NM_001354800.1:c.1307T>A