Canonical Allele Identifier: PA209996
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206978
ClinVar RCV Id: RCV000189127 RCV000417104 RCV000195526 RCV002433854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ser987Ile
CA209995
NM_001040142.2:c.2960G>T