Canonical Allele Identifier: PA2826014211
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 530419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ala1910Val
CA59797796
NM_001165964.3:c.5729C>T