Canonical Allele Identifier: PA2825738453
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436929
ClinVar RCV Id: RCV000501554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Pro981Ser
CA363630171
NM_001130066.2:c.2941C>T