Canonical Allele Identifier: PA1139722377
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 946946
ClinVar RCV Id: RCV001217911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Leu870Val
CA363626129
NM_006772.3:c.2608C>G