Canonical Allele Identifier: PA2826009449
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1480447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Arg617Gly
CA349067458
NM_001165963.4:c.1849A>G