Canonical Allele Identifier: PA2826012468
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206784
ClinVar RCV Id: RCV000188892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Val829Ile
CA317299
NM_001165964.3:c.2485G>A