Canonical Allele Identifier: PA2825355738
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1702747
ClinVar RCV Id: RCV002279065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Glu1228Lys
CA349027468
NM_001040142.2:c.3682G>A