Canonical Allele Identifier: PA2827788874
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1175963
ClinVar RCV Id: RCV001531323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Lys1228_Val1229del
CA2499215174
NM_001353960.2:c.3682_3687del