Canonical Allele Identifier: PA2827937095
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2632567
ClinVar RCV Id: RCV003416862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg32Pro
CA367398967
NM_001354801.1:c.95G>C