Canonical Allele Identifier: PA2827937029
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447389
ClinVar RCV Id: RCV000516995 RCV004527383
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe423Ser
CA367397256
NM_001354800.1:c.1268T>C