Canonical Allele Identifier: PA2825738438
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000410
ClinVar RCV Id: RCV001296534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Phe965Leu
CA363629700
NM_001130066.2:c.2893T>C
CA363629732
NM_001130066.2:c.2895C>A
CA363629738
NM_001130066.2:c.2895C>G