Canonical Allele Identifier: PA913195316
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 624244
ClinVar RCV Id: RCV000762408
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser842Tyr
CA363625668
NM_006772.3:c.2525C>A