Canonical Allele Identifier: PA2580350997
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804329
ClinVar RCV Id: RCV002469630
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Cys282Ser
CA363684451
NM_006772.3:c.844T>A
CA363684462
NM_006772.3:c.845G>C