Canonical Allele Identifier: PA2573254292
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392908
ClinVar RCV Id: RCV001882293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser858Asn
CA3758920
NM_006772.3:c.2573G>A