Canonical Allele Identifier: PA2826011854
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801479
ClinVar RCV Id: RCV002463568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gly355Asp
CA349071358
NM_001165964.3:c.1064G>A