Canonical Allele Identifier: PA2830123315
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3026940
ClinVar RCV Id: RCV003887333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp197Ala
CA367401419
NM_033508.3:c.590A>C