Canonical Allele Identifier: PA2827937368
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Leu64Pro
CA213723
NM_001354803.2:c.191T>C