Canonical Allele Identifier: PA2580351067
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1983021
ClinVar RCV Id: RCV002785722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Arg884Gln
CA363626395
NM_006772.3:c.2651G>A