Canonical Allele Identifier: PA2830122408
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 910353
ClinVar RCV Id: RCV001162074 RCV001162075 RCV001162073 RCV001164091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu422Gly
CA367397281
NM_033507.3:c.1265A>G