Canonical Allele Identifier: PA645471778
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436929
ClinVar RCV Id: RCV000501554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Pro995Ser
CA363630171
NM_006772.3:c.2983C>T