Canonical Allele Identifier: PA2826010371
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1069950
ClinVar RCV Id: RCV001381948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val1428Asp
CA349049864
NM_001165963.4:c.4283T>A