Canonical Allele Identifier: PA2827936551
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628363
ClinVar RCV Id: RCV003397218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe148Ser
CA367401964
NM_001354800.1:c.443T>C