Allele Registry

Canonical Allele Identifier: PA645471523

Gene: SYNGAP1 HGNC NCBI

ClinVar Allele:

370419

ClinVar RCV:

RCV000433653

ClinVar Variation:

391294

HGVS (amino-acid)	Matching Registered Transcripts
NP_006763.2:p.Trp308Arg	CA16605532 NM_006772.3:c.922T>C CA363685104 NM_006772.3:c.922T>A