Canonical Allele Identifier: PA2827790682
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2443596
ClinVar RCV Id: RCV003152203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Pro1028Leu
CA349065614
NM_001353961.2:c.3083C>T