Canonical Allele Identifier: PA2827936412
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700673
ClinVar RCV Id: RCV002285551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met41Arg
CA367403469
NM_001354800.1:c.122T>G