Canonical Allele Identifier: PA2499274885
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1055027
ClinVar RCV Id: RCV001363628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser604Leu
CA363693573
NM_006772.3:c.1811C>T