Canonical Allele Identifier: PA2827783681
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ala1657Val
CA266120
NM_001353957.2:c.4970C>T