Canonical Allele Identifier: PA2579983002
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691827
ClinVar RCV Id: RCV003494024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala208Pro
CA367401320
NM_000162.5:c.622G>C