Canonical Allele Identifier: PA2825357960
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207093
ClinVar RCV Id: RCV000189248
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Ala240Phe
CA318223
NM_001040143.2:c.718_719delinsTT