Canonical Allele Identifier: PA2827936449
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2779779
ClinVar RCV Id: RCV003665331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg63His
CA4239706
NM_001354800.1:c.188G>A