Canonical Allele Identifier: PA2827937163
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 981653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Met56Thr
CA367398600
NM_001354801.1:c.167T>C