Canonical Allele Identifier: PA2825738318
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 537003
ClinVar RCV Id: RCV000645742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Ser822Gly
CA363625550
NM_001130066.2:c.2464A>G