Canonical Allele Identifier: PA2827759704
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1203729
ClinVar RCV Id: RCV001569863 RCV001866017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ala1300Val
CA349053215
NM_001353949.2:c.3899C>T