Canonical Allele Identifier: PA2579976304
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2098687
ClinVar RCV Id: RCV003031070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Pro284Leu
CA367400423
NM_000162.5:c.851C>T