Canonical Allele Identifier: PA2580490747
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807282
ClinVar RCV Id: RCV002475239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Cys130Phe
CA367402158
NM_033507.3:c.389G>T