Allele Registry

Canonical Allele Identifier: PA2499274893

Gene: SYNGAP1 HGNC NCBI

ClinVar Variation Id: 1000410

HGVS (amino-acid)	Matching Registered Transcripts
NP_006763.2:p.Phe979Leu	CA363629700 NM_006772.3:c.2935T>C CA363629732 NM_006772.3:c.2937C>A CA363629738 NM_006772.3:c.2937C>G