Canonical Allele Identifier: PA2573254093
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509894
ClinVar RCV Id: RCV002011369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Thr305Ala
CA363685021
NM_006772.3:c.913A>G