Canonical Allele Identifier: PA2827777297
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ala1429Pro
CA284958
NM_001353954.2:c.4285G>C