Canonical Allele Identifier: PA2825738338
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484973
ClinVar RCV Id: RCV002008314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Ser847Leu
CA3758921
NM_001130066.2:c.2540C>T