Canonical Allele Identifier: PA128709
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 29886
ClinVar RCV Id: RCV000189138 RCV000118248 RCV000022767 RCV000806278 RCV001847619 RCV002319425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Glu1211Lys
CA128708
NM_021007.3:c.3631G>A