Canonical Allele Identifier: PA2580351000
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2122760
ClinVar RCV Id: RCV003047028
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Met289Val
CA363684626
NM_006772.3:c.865A>G