Canonical Allele Identifier: PA2825737890
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 981381
ClinVar RCV Id: RCV001260777 RCV003153963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Trp308Cys
CA363685127
NM_001130066.2:c.924G>C
CA363685131
NM_001130066.2:c.924G>T