Canonical Allele Identifier: PA2579982999
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala208Thr
CA367401322
NM_000162.5:c.622G>A