Canonical Allele Identifier: PA2827765770
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805382
ClinVar RCV Id: RCV000992879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Val1158Ala
CA349056680
NM_001353950.2:c.3473T>C