Canonical Allele Identifier: PA2827936948
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser383Pro
CA367398737
NM_001354800.1:c.1147T>C