Canonical Allele Identifier: PA2825738406
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165090
ClinVar RCV Id: RCV003082438 RCV003404079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.His931Gln
CA363628788
NM_001130066.2:c.2793T>A
CA363628789
NM_001130066.2:c.2793T>G