Canonical Allele Identifier: PA658668930
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg64Cys
CA4239707
NM_033507.3:c.190C>T