Canonical Allele Identifier: PA2827789492
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Val1601Met
CA284988
NM_001353960.2:c.4801G>A