Canonical Allele Identifier: PA2579982802
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2779779
ClinVar RCV Id: RCV003665331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg63His
CA4239706
NM_000162.5:c.188G>A