Canonical Allele Identifier: PA2579980387
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807281
ClinVar RCV Id: RCV002475238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu236Val
CA367400733
NM_000162.5:c.707A>T