Canonical Allele Identifier: PA2830122319
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1300949
ClinVar RCV Id: RCV001733092 RCV002222722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val409Met
CA367398343
NM_033507.3:c.1225G>A