Canonical Allele Identifier: PA2573254287
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395978
ClinVar RCV Id: RCV001887316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Val841Ala
CA363625656
NM_006772.3:c.2522T>C