Canonical Allele Identifier: PA2826010125
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1175963
ClinVar RCV Id: RCV001531323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Lys1257_Val1258del
CA2499215174
NM_001165963.4:c.3769_3774del