Canonical Allele Identifier: PA2827765383
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 429403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Val1005Met
CA59787454
NM_001353950.2:c.3013G>A