Canonical Allele Identifier: PA913195297
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 635755
ClinVar RCV Id: RCV000787271 RCV003226976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Cys282Arg
CA363684454
NM_006772.3:c.844T>C