Canonical Allele Identifier: PA2827936586
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679554
ClinVar RCV Id: RCV002227433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly162Asp
CA367401806
NM_001354800.1:c.485G>A