Canonical Allele Identifier: PA645459516
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 211073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp125Asn
CA206547
NM_033507.3:c.373G>A