Canonical Allele Identifier: PA2826010207
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1385928
ClinVar RCV Id: RCV001889064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Leu1318Val
CA349053111
NM_001165963.4:c.3952C>G