Canonical Allele Identifier: PA213849
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36255
ClinVar RCV Id: RCV000029918 RCV002463610
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu256Asp
CA213848
NM_000162.5:c.768G>C
CA367400599
NM_000162.5:c.768G>T