Canonical Allele Identifier: PA2825353522
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 934399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Leu210Gln
CA349017376
NM_001040142.2:c.629T>A