Canonical Allele Identifier: PA2826009281
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1311030
ClinVar RCV Id: RCV001758539
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala442Gly
CA349070502
NM_001165963.4:c.1325C>G