Canonical Allele Identifier: PA2825737877
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3010802
ClinVar RCV Id: RCV003862441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.[Thr294Ile;Ser296Ala]
CA2695202911
NM_001130066.2:c.881_886delinsTCACCG