Canonical Allele Identifier: PA2830124016
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val426Gly
CA367397199
NM_033508.3:c.1277T>G