Canonical Allele Identifier: PA2826009993
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805382
ClinVar RCV Id: RCV000992879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val1169Ala
CA349056680
NM_001165963.4:c.3506T>C