Canonical Allele Identifier: PA2825737868
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2826106
ClinVar RCV Id: RCV003616444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Asp287Ala
CA363684582
NM_001130066.2:c.860A>C