Canonical Allele Identifier: PA1139735370
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 981653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Met71Thr
CA367398600
NM_001354803.2:c.212T>C