Canonical Allele Identifier: PA2830123890
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233998
ClinVar RCV Id: RCV004527574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val388Ala
CA367398657
NM_033508.3:c.1163T>C