Canonical Allele Identifier: PA2827759351
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2313708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Thr1211Ile
CA349055889
NM_001353949.2:c.3632C>T