Canonical Allele Identifier: PA658707435
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 496120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val1538Ile
CA1942758
NM_001165963.4:c.4612G>A