Canonical Allele Identifier: PA2827789855
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1036382
ClinVar RCV Id: RCV001339386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Trp1783Ser
CA349067588
NM_001353960.2:c.5348G>C