Canonical Allele Identifier: PA2825737942
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218691
ClinVar RCV Id: RCV000203123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Ser385Trp
CA249323
NM_001130066.2:c.1154C>G