Canonical Allele Identifier: PA2827775411
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1310742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Val126Ile
CA349076779
NM_001353954.2:c.376G>A