Canonical Allele Identifier: PA2827776948
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ala1224Pro
CA303346
NM_001353954.2:c.3670G>C