Canonical Allele Identifier: PA2741997512
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2502089
ClinVar RCV Id: RCV003228508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala189Pro
CA367401562
NM_033507.3:c.565G>C