Canonical Allele Identifier: PA2826011105
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1036382
ClinVar RCV Id: RCV001339386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Trp1812Ser
CA349067588
NM_001165963.4:c.5435G>C