Canonical Allele Identifier: PA2826011157
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1685088
ClinVar RCV Id: RCV002248180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Pro1844Leu
CA349065582
NM_001165963.4:c.5531C>T