Canonical Allele Identifier: PA2741868029
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2632567
ClinVar RCV Id: RCV003416862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg47Pro
CA367398967
NM_001354803.2:c.140G>C