Canonical Allele Identifier: PA2499274828
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1204186
ClinVar RCV Id: RCV001570465
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Arg279Trp
CA363684399
NM_006772.3:c.835C>T