Canonical Allele Identifier: PA2573089052
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1337384
ClinVar RCV Id: RCV001820398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser873Arg
CA363626170
NM_006772.3:c.2617A>C
CA363626185
NM_006772.3:c.2619C>A
CA363626186
NM_006772.3:c.2619C>G