Canonical Allele Identifier: PA2741932793
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2965590
ClinVar RCV Id: RCV003825740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Pro298Ser
CA363684838
NM_006772.3:c.892C>T