Canonical Allele Identifier: PA2827936612
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36227
ClinVar RCV Id: RCV000029890 RCV002463599
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly178Arg
CA213798
NM_001354800.1:c.532G>A
CA367401653
NM_001354800.1:c.532G>C