Canonical Allele Identifier: PA645471786
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225899
ClinVar RCV Id: RCV000211105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Ser1165Leu
CA10576135
NM_006772.3:c.3494C>T