Canonical Allele Identifier: PA2825358137
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1320536
ClinVar RCV Id: RCV001776515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Asn359Ser
CA1939757
NM_001040143.2:c.1076A>G