Canonical Allele Identifier: PA2827937347
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Leu50Pro
CA213749
NM_001354802.1:c.149T>C