Canonical Allele Identifier: PA915983563
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 708250
ClinVar RCV Id: RCV000879476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Asn1213Ser
CA3759081
NM_006772.3:c.3638A>G