Canonical Allele Identifier: PA2827789188
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ala1412Pro
CA284958
NM_001353960.2:c.4234G>C