Canonical Allele Identifier: PA2827936977
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 981653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met393Thr
CA367398600
NM_001354800.1:c.1178T>C