Canonical Allele Identifier: PA2830123469
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1172895
ClinVar RCV Id: RCV001527031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asn230Asp
CA367400772
NM_033508.3:c.688A>G