Canonical Allele Identifier: PA2741932923
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2904850
ClinVar RCV Id: RCV003615573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Arg884Trp
CA137072904
NM_006772.3:c.2650C>T