Canonical Allele Identifier: PA658674270
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 448636
ClinVar RCV Id: RCV000516746 RCV001522591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Arg1221Gln
CA137075371
NM_006772.3:c.3662G>A