Canonical Allele Identifier: PA2499274853
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037885
ClinVar RCV Id: RCV001341108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Arg890His
CA3758934
NM_006772.3:c.2669G>A