Canonical Allele Identifier: PA2825738327
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2042462
ClinVar RCV Id: RCV002917497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Gly836Arg
CA363625803
NM_001130066.2:c.2506G>A
CA363625806
NM_001130066.2:c.2506G>C