Canonical Allele Identifier: PA2580490794
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2499721
ClinVar RCV Id: RCV003223813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg193Ser
CA367401516
NM_033507.3:c.579A>T
CA367401517
NM_033507.3:c.579A>C