Canonical Allele Identifier: PA2827936919
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2578348
ClinVar RCV Id: RCV003326074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val374Glu
CA367398869
NM_001354800.1:c.1121T>A