Canonical Allele Identifier: PA2741932917
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2966994
ClinVar RCV Id: RCV003829128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Val841Met
CA363625652
NM_006772.3:c.2521G>A