Canonical Allele Identifier: PA915983064
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 809920
ClinVar RCV Id: RCV000998585 RCV001858883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ala301Thr
CA363684928
NM_006772.3:c.901G>A