Canonical Allele Identifier: PA2825737872
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2122760
ClinVar RCV Id: RCV003047028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Met289Val
CA363684626
NM_001130066.2:c.865A>G