Canonical Allele Identifier: PA2828473890
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1507589
ClinVar RCV Id: RCV002048109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Leu222Ile
CA349017507
NM_001371247.1:c.664C>A