Canonical Allele Identifier: PA2579982973
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1756314
ClinVar RCV Id: RCV002362470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala232Asp
CA367400762
NM_000162.5:c.695C>A