Canonical Allele Identifier: PA2580351068
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2167465
ClinVar RCV Id: RCV003092128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ala886Val
CA3758929
NM_006772.3:c.2657C>T