Canonical Allele Identifier: PA2827937171
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2734991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg60Cys
CA4239418
NM_001354801.1:c.178C>T