Canonical Allele Identifier: PA2830123559
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36257
ClinVar RCV Id: RCV000029920 RCV002463611
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe259Ser
CA213852
NM_033508.3:c.776T>C