Canonical Allele Identifier: PA2579983033
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2502089
ClinVar RCV Id: RCV003228508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala188Pro
CA367401562
NM_000162.5:c.562G>C