Canonical Allele Identifier: PA2827779827
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805382
ClinVar RCV Id: RCV000992879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val1157Ala
CA349056680
NM_001353955.2:c.3470T>C