Canonical Allele Identifier: PA2830123593
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 994611
ClinVar RCV Id: RCV001288182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp273Glu
CA367400481
NM_033508.3:c.819C>G
CA367400482
NM_033508.3:c.819C>A