Canonical Allele Identifier: PA2579976222
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser383Pro
CA367398737
NM_000162.5:c.1147T>C