Canonical Allele Identifier: PA2825737800
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375528
ClinVar RCV Id: RCV000417030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Arg170Gln
CA16044319
NM_001130066.2:c.509G>A