Canonical Allele Identifier: PA2579976342
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1187444
ClinVar RCV Id: RCV001546887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Pro145Leu
CA367401987
NM_000162.5:c.434C>T