Canonical Allele Identifier: PA2580229272
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg85Trp
CA367397271
NM_001354801.1:c.253C>T