Canonical Allele Identifier: PA658817969
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 537003
ClinVar RCV Id: RCV000645742
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser836Gly
CA363625550
NM_006772.3:c.2506A>G