Canonical Allele Identifier: PA2827754299
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Val1630Met
CA284988
NM_001353948.2:c.4888G>A