Canonical Allele Identifier: PA2825356276
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3066121
ClinVar RCV Id: RCV003991125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Val1432del
CA2740097952
NM_001040142.2:c.4295_4297del