Canonical Allele Identifier: PA2827936650
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met202Val
CA213808
NM_001354800.1:c.604A>G