Canonical Allele Identifier: PA2827774067
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2651498
ClinVar RCV Id: RCV003429348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ala1292Val
CA1942864
NM_001353952.2:c.3875C>T