Canonical Allele Identifier: PA916036855
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 496120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Val724Ile
CA1942758
NM_001353961.2:c.2170G>A