Canonical Allele Identifier: PA658669044
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 450262
ClinVar Variation Id: 1045215
ClinVar RCV Id: RCV001349584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asn255Lys
CA367400610
NM_033507.3:c.765T>G
CA367400611
NM_033507.3:c.765T>A