Canonical Allele Identifier: PA2579982806
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg63Cys
CA4239707
NM_000162.5:c.187C>T