Canonical Allele Identifier: PA2825353872
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1343156
ClinVar RCV Id: RCV001843757 RCV002319730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Arg379His
CA349021050
NM_001040142.2:c.1136G>A