Allele Registry

Canonical Allele Identifier: PA2825737811

Gene: SYNGAP1 HGNC NCBI

ClinVar RCV:

RCV000416992

ClinVar Variation:

375527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123538.1:p.Ala195Pro	CA16044320 NM_001130066.2:c.583G>C