Canonical Allele Identifier: PA2826013915
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2057676
ClinVar RCV Id: RCV002942053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Pro1731Leu
CA349068303
NM_001165964.3:c.5192C>T