Canonical Allele Identifier: PA2580351063
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2089808
ClinVar RCV Id: RCV003005697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser840Cys
CA363625627
NM_006772.3:c.2518A>T