Canonical Allele Identifier: PA2829675786
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 663230
ClinVar RCV Id: RCV000821070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Leu1298Val
CA349053265
NM_006920.6:c.3892C>G