Canonical Allele Identifier: PA2830123127
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe151Leu
CA367401920
NM_033508.3:c.453T>G
CA367401922
NM_033508.3:c.453T>A
CA367401929
NM_033508.3:c.451T>C