Canonical Allele Identifier: PA2499251709
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1069950
ClinVar RCV Id: RCV001381948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Val614Asp
CA349049864
NM_001353961.2:c.1841T>A