Canonical Allele Identifier: PA2828473702
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1693057
ClinVar RCV Id: RCV002259484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Tyr110His
CA349011583
NM_001371247.1:c.328T>C