Canonical Allele Identifier: PA2830123099
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628363
ClinVar RCV Id: RCV003397218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe147Ser
CA367401964
NM_033508.3:c.440T>C