Canonical Allele Identifier: PA2827788838
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ala1207Pro
CA303346
NM_001353960.2:c.3619G>C