Canonical Allele Identifier: PA645403687
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 429403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val1016Met
CA59787454
NM_001165963.4:c.3046G>A