Canonical Allele Identifier: PA2827937325
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807286
ClinVar RCV Id: RCV002475243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Lys34Asn
CA367398236
NM_001354802.1:c.102G>T
CA367398238
NM_001354802.1:c.102G>C