Canonical Allele Identifier: PA2825738470
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1901716
ClinVar RCV Id: RCV002576760
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Pro1020Ala
CA363631172
NM_001130066.2:c.3058C>G