Canonical Allele Identifier: PA2830122680
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804838
ClinVar RCV Id: RCV000992040 RCV002464351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met40Val
CA367403472
NM_033508.3:c.118A>G