Canonical Allele Identifier: PA2573254302
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436537
ClinVar RCV Id: RCV001987410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Arg890Cys
CA363626538
NM_006772.3:c.2668C>T