Canonical Allele Identifier: PA2827936413
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met41Thr
CA16609270
NM_001354800.1:c.122T>C