Canonical Allele Identifier: PA2827790037
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2014067
ClinVar RCV Id: RCV002861311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Leu1902Ser
CA349063832
NM_001353960.2:c.5705T>C