Canonical Allele Identifier: PA317932
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206988
ClinVar RCV Id: RCV000189137 RCV000795173 RCV002288794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Glu1162Val
CA317930
NM_021007.3:c.3485A>T