Canonical Allele Identifier: PA2827936620
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1447652
ClinVar RCV Id: RCV001996845 RCV002282665 RCV003159566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu184Pro
CA367401589
NM_001354800.1:c.551T>C