Canonical Allele Identifier: PA2827779659
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 429403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val1004Met
CA59787454
NM_001353955.2:c.3010G>A