Canonical Allele Identifier: PA2825359947
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1803061
ClinVar RCV Id: RCV002466358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Phe1476Ile
CA349034281
NM_001040143.2:c.4426T>A