Canonical Allele Identifier: PA2825738346
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1337384
ClinVar RCV Id: RCV001820398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Ser859Arg
CA363626170
NM_001130066.2:c.2575A>C
CA363626185
NM_001130066.2:c.2577C>A
CA363626186
NM_001130066.2:c.2577C>G