Canonical Allele Identifier: PA2827936601
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129143
ClinVar RCV Id: RCV000117130 RCV002336252 RCV003318498
ClinVar Variation Id: 3024423
ClinVar RCV Id: RCV003883459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly175Arg
CA231137
NM_001354800.1:c.523G>A
CA367401686
NM_001354800.1:c.523G>C