Canonical Allele Identifier: PA916039375
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 418228
ClinVar RCV Id: RCV000479890 RCV002431386 RCV003493592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Asp41Asn
CA16618466
NM_001354803.2:c.121G>A