Canonical Allele Identifier: PA2826012895
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805382
ClinVar RCV Id: RCV000992879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Val1141Ala
CA349056680
NM_001165964.3:c.3422T>C