Canonical Allele Identifier: PA2580351102
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900229
ClinVar RCV Id: RCV002582953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Tyr1219His
CA363637145
NM_006772.3:c.3655T>C