Canonical Allele Identifier: PA2827782373
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206784
ClinVar RCV Id: RCV000188892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Val829Ile
CA317299
NM_001353957.2:c.2485G>A