Canonical Allele Identifier: PA2827754300
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2715522
ClinVar RCV Id: RCV003590623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Val1630Ala
CA349070509
NM_001353948.2:c.4889T>C