Canonical Allele Identifier: PA2825737787
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2436908
ClinVar RCV Id: RCV003140828
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Asp151Glu
CA363680692
NM_001130066.2:c.453C>A
CA363680693
NM_001130066.2:c.453C>G