Canonical Allele Identifier: PA2579975098
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Trp167Arg
CA367401768
NM_000162.5:c.499T>C
CA367401770
NM_000162.5:c.499T>A