Canonical Allele Identifier: PA645471523
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391294
ClinVar RCV Id: RCV000433653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Trp308Arg
CA16605532
NM_006772.3:c.922T>C
CA363685104
NM_006772.3:c.922T>A