Canonical Allele Identifier: PA1139722381
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 934469
ClinVar RCV Id: RCV001202867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ala901Val
CA363626736
NM_006772.3:c.2702C>T