Canonical Allele Identifier: PA2825738626
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1476244
ClinVar RCV Id: RCV001995440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Arg1198Trp
CA363637071
NM_001130066.2:c.3592C>T