Canonical Allele Identifier: PA2827936741
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995372
ClinVar RCV Id: RCV001289443 RCV002463807 RCV003446687
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly246Arg
CA367400664
NM_001354800.1:c.736G>C
CA367400665
NM_001354800.1:c.736G>A