Canonical Allele Identifier: PA2499274865
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1029090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Gly991Arg
CA137073211
NM_006772.3:c.2971G>A
CA363630058
NM_006772.3:c.2971G>C