Canonical Allele Identifier: PA2580351073
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165090
ClinVar RCV Id: RCV003082438 RCV003404079
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.His945Gln
CA363628788
NM_006772.3:c.2835T>A
CA363628789
NM_006772.3:c.2835T>G