Canonical Allele Identifier: PA2579982906
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2499721
ClinVar RCV Id: RCV003223813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg192Ser
CA367401516
NM_000162.5:c.576A>T
CA367401517
NM_000162.5:c.576A>C