Canonical Allele Identifier: PA2829675441
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 429403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Val1005Met
CA59787454
NM_006920.6:c.3013G>A