Canonical Allele Identifier: PA2825738437
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 624245
ClinVar RCV Id: RCV000762409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Phe962Leu
CA363629640
NM_001130066.2:c.2884T>C
CA363629662
NM_001130066.2:c.2886T>A
CA363629663
NM_001130066.2:c.2886T>G