Canonical Allele Identifier: PA2828475720
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 410982
ClinVar RCV Id: RCV000469153 RCV001270400 RCV002510575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Arg1319Trp
CA1940198
NM_001371247.1:c.3955C>T