Canonical Allele Identifier: PA2579982709
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807280
ClinVar RCV Id: RCV002475237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala370Pro
CA367398963
NM_000162.5:c.1108G>C