Canonical Allele Identifier: PA2825737866
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804329
ClinVar RCV Id: RCV002469630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Cys282Ser
CA363684451
NM_001130066.2:c.844T>A
CA363684462
NM_001130066.2:c.845G>C