Canonical Allele Identifier: PA2825738450
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1029090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Gly977Arg
CA137073211
NM_001130066.2:c.2929G>A
CA363630058
NM_001130066.2:c.2929G>C