Canonical Allele Identifier: PA2825738629
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900229
ClinVar RCV Id: RCV002582953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Tyr1203His
CA363637145
NM_001130066.2:c.3607T>C