Canonical Allele Identifier: PA913195321
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 624245
ClinVar RCV Id: RCV000762409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Phe976Leu
CA363629640
NM_006772.3:c.2926T>C
CA363629662
NM_006772.3:c.2928T>A
CA363629663
NM_006772.3:c.2928T>G