Canonical Allele Identifier: PA2827936561
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe152Leu
CA367401920
NM_001354800.1:c.456T>G
CA367401922
NM_001354800.1:c.456T>A
CA367401929
NM_001354800.1:c.454T>C