Canonical Allele Identifier: PA2826010172
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 836073
ClinVar RCV Id: RCV001037109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val1294Phe
CA349053549
NM_001165963.4:c.3880G>T