Canonical Allele Identifier: PA2826258057
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2011463
ClinVar RCV Id: RCV002851277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Leu125Val
CA349076791
NM_001202435.3:c.373T>G