Canonical Allele Identifier: PA2580351064
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2042462
ClinVar RCV Id: RCV002917497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Gly850Arg
CA363625803
NM_006772.3:c.2548G>A
CA363625806
NM_006772.3:c.2548G>C