Canonical Allele Identifier: PA2826260664
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2443596
ClinVar RCV Id: RCV003152203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Pro1842Leu
CA349065614
NM_001202435.3:c.5525C>T