Canonical Allele Identifier: PA2827936599
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1691788
ClinVar RCV Id: RCV002255216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala173Pro
CA367401703
NM_001354800.1:c.517G>C