Canonical Allele Identifier: PA2830123194
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Trp166Arg
CA367401768
NM_033508.3:c.496T>C
CA367401770
NM_033508.3:c.496T>A