Canonical Allele Identifier: PA2825354067
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 812987
ClinVar RCV Id: RCV001003953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Val424Leu
CA349022252
NM_001040142.2:c.1270G>C
CA349022254
NM_001040142.2:c.1270G>T