Canonical Allele Identifier: PA645461044
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu387Pro
CA213723
NM_033507.3:c.1160T>C