Canonical Allele Identifier: PA2579980674
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys382Arg
CA367398754
NM_000162.5:c.1144T>C