Canonical Allele Identifier: PA2827936638
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2499721
ClinVar RCV Id: RCV003223813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg192Ser
CA367401516
NM_001354800.1:c.576A>T
CA367401517
NM_001354800.1:c.576A>C