Canonical Allele Identifier: PA2580490785
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1746353
ClinVar RCV Id: RCV002344350 RCV003883199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly176Val
CA367401683
NM_033507.3:c.527G>T