Canonical Allele Identifier: PA2579982516
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg422Trp
CA367397271
NM_000162.5:c.1264C>T