Canonical Allele Identifier: PA2825737879
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2965590
ClinVar RCV Id: RCV003825740
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Pro298Ser
CA363684838
NM_001130066.2:c.892C>T