Canonical Allele Identifier: PA2741932921
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2572755
ClinVar RCV Id: RCV003314869 RCV003615949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser876Leu
CA363626234
NM_006772.3:c.2627C>T