Canonical Allele Identifier: PA2580351066
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1794068
ClinVar RCV Id: RCV002428566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Thr878Ala
CA363626259
NM_006772.3:c.2632A>G