Canonical Allele Identifier: PA2830123889
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435300
ClinVar RCV Id: RCV000499682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val388Leu
CA367398665
NM_033508.3:c.1162G>C