Canonical Allele Identifier: PA2827770866
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805382
ClinVar RCV Id: RCV000992879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Val1158Ala
CA349056680
NM_001353951.2:c.3473T>C