Canonical Allele Identifier: PA2828470557
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1705326
ClinVar RCV Id: RCV002283640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Val238Ala
CA349017790
NM_001371246.1:c.713T>C