Canonical Allele Identifier: PA2825737869
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1700054
ClinVar RCV Id: RCV002274303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Asp287His
CA363684576
NM_001130066.2:c.859G>C