Allele Registry

Canonical Allele Identifier: PA645471521

Gene: SYNGAP1 HGNC NCBI

ClinVar RCV:

RCV000416992

ClinVar Variation:

375527

HGVS (amino-acid)	Matching Registered Transcripts
NP_006763.2:p.Ala195Pro	CA16044320 NM_006772.3:c.583G>C