Canonical Allele Identifier: PA2825737871
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2572204
ClinVar RCV Id: RCV003314089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Asp288Asn
CA3758576
NM_001130066.2:c.862G>A