Canonical Allele Identifier: PA2825738319
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1377909
ClinVar RCV Id: RCV001880895 RCV003228012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Asn824Lys
CA363625599
NM_001130066.2:c.2472C>A
CA363625601
NM_001130066.2:c.2472C>G