Canonical Allele Identifier: PA2827937376
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435300
ClinVar RCV Id: RCV000499682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val67Leu
CA367398665
NM_001354803.2:c.199G>C