Canonical Allele Identifier: PA2579974867
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val199Met
CA367401409
NM_000162.5:c.595G>A